These terms and conditions govern your use of the website alphaminr.com and its related
services.
These Terms and Conditions (“Terms”) are a binding contract between you and Alphaminr,
(“Alphaminr”, “we”, “us” and “service”). You must agree to and accept the Terms. These Terms
include the provisions in this document as well as those in the Privacy Policy. These terms may
be modified at any time.
Subscription
Your subscription will be on a month to month basis and automatically renew every month. You may
terminate your subscription at any time through your account.
Fees
We will provide you with advance notice of any change in fees.
Usage
You represent that you are of legal age to form a binding contract. You are responsible for any
activity associated with your account. The account can be logged in at only one computer at a
time.
The Services are intended for your own individual use. You shall only use the Services in a
manner that complies with all laws. You may not use any automated software, spider or system to
scrape data from Alphaminr.
Limitation of Liability
Alphaminr is not a financial advisor and does not provide financial advice of any kind. The
service is provided “As is”. The materials and information accessible through the Service are
solely for informational purposes. While we strive to provide good information and data, we make
no guarantee or warranty as to its accuracy.
TO THE EXTENT PERMITTED BY APPLICABLE LAW, UNDER NO CIRCUMSTANCES SHALL ALPHAMINR BE LIABLE TO
YOU FOR DAMAGES OF ANY KIND, INCLUDING DAMAGES FOR INVESTMENT LOSSES, LOSS OF DATA, OR ACCURACY
OF DATA, OR FOR ANY AMOUNT, IN THE AGGREGATE, IN EXCESS OF THE GREATER OF (1) FIFTY DOLLARS OR
(2) THE AMOUNTS PAID BY YOU TO ALPHAMINR IN THE SIX MONTH PERIOD PRECEDING THIS APPLICABLE
CLAIM. SOME STATES DO NOT ALLOW THE EXCLUSION OR LIMITATION OF INCIDENTAL OR CONSEQUENTIAL OR
CERTAIN OTHER DAMAGES, SO THE ABOVE LIMITATION AND EXCLUSIONS MAY NOT APPLY TO YOU.
If any provision of these Terms is found to be invalid under any applicable law, such provision
shall not affect the validity or enforceability of the remaining provisions herein.
Privacy Policy
This privacy policy describes how we (“Alphaminr”) collect, use, share and protect your personal
information when we provide our service (“Service”). This Privacy Policy explains how
information is collected about you either directly or indirectly. By using our service, you
acknowledge the terms of this Privacy Notice. If you do not agree to the terms of this Privacy
Policy, please do not use our Service. You should contact us if you have questions about it. We
may modify this Privacy Policy periodically.
Personal Information
When you register for our Service, we collect information from you such as your name, email
address and credit card information.
Usage
Like many other websites we use “cookies”, which are small text files that are stored on your
computer or other device that record your preferences and actions, including how you use the
website. You can set your browser or device to refuse all cookies or to alert you when a cookie
is being sent. If you delete your cookies, if you opt-out from cookies, some Services may not
function properly. We collect information when you use our Service. This includes which pages
you visit.
Sharing of Personal Information
We use Google Analytics and we use Stripe for payment processing. We will not share the
information we collect with third parties for promotional purposes.
We may share personal information with law enforcement as required or permitted by law.
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the quarterly period ended
June 30,
2025
OR
☐
TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from
to
.
Commission File Number:
0-19961
ORTHOFIX MEDICAL INC.
(Exact name of registrant as specified in its charter)
Delaware
98-1340767
(State or other jurisdiction of
incorporation or organization)
(I.R.S. Employer
Identification No.)
3451 Plano Parkway
,
Lewisville
,
Texas
75056
(Address of principal executive offices)
(Zip Code)
(
214
)
937-2000
(Registrant's telephone number, including area code)
Not applicable
(Former name, former address and former fiscal year, if changed since last report)
Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
☒
Yes
☐
No
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).
☒
Yes
☐
No
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See the definitions of "large accelerated filer," "accelerated filer," "smaller reporting company," and "emerging growth company" in Rule 12b-2 of the Exchange Act.
Large Accelerated filer
☐
Accelerated filer
☒
Non-Accelerated filer
☐
Smaller Reporting Company
☐
Emerging Growth Company
☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).
☐
Yes
☒
No
As of July 31, 2025,
39,494,265
shares of common stock were issued and outstanding.
Securities registered pursuant to Section 12(b) of the Act:
This Quarterly Report contains forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), and Section 27A of the Securities Act of 1933, as amended (the "Securities Act"), relating to our business and financial outlook, which are based on our current beliefs, assumptions, expectations, estimates, forecasts, and projections. All statements, other than statements of historical fact, contained in this report, are forward-looking statements. In some cases, you can identify forward-looking statements by terms such as "may," "will," "should," "expects," "plans," "anticipates," "believes," "estimates," "projects," "intends," "predicts," "potential," "positioned," "deliver," or "continue" or the negative version of those terms and other similar expressions. Forward-looking statements include, but are not limited to, statements about:
•
our intentions, beliefs, and expectations regarding our operations, sales, expenses, and future financial performance;
•
our operating results;
•
our intentions, beliefs, and expectations regarding the anticipated benefits of the merger with SeaSpine Holdings Corporation ("SeaSpine"), including the anticipated cross-selling opportunities from the merger;
•
our plans for future products and enhancements of existing products;
•
anticipated growth and trends in our business;
•
the timing of and our ability to maintain and obtain regulatory clearances or approvals;
•
our belief that our cash and cash equivalents, investments, and access to our credit facilities will be sufficient to satisfy our anticipated cash requirements;
•
our expectations regarding our revenues, customers, and distributors;
•
our expectations regarding our costs, suppliers, and manufacturing abilities;
•
our beliefs and expectations regarding our market penetration and expansion efforts;
•
our anticipated trends and challenges in the markets in which we operate; and
•
our expectations and beliefs regarding, and the impact of, investigations, claims, and litigation.
Forward-looking statements are not guarantees of future performance and involve risks, uncertainties, estimates, and assumptions. Any or all forward-looking statements that we make may turn out to be wrong (due to inaccurate assumptions that we make or otherwise), and our actual outcomes and results may differ materially from those expressed in forward-looking statements. Potential risks and uncertainties that could cause actual results to differ materially include, but are not limited to, those set forth in Part I, Item 1A under the heading
Risk Factors
of our Annual Report on Form 10-K for the year ended December 31, 2024 ("2024 10-K"); Part II, Item 7
Management's Discussion and Analysis of Financial Condition and Results of Operations
of the 2024 10-K
;
and elsewhere throughout the 2024 10-K, and in our reports filed with the U.S. Securities and Exchange Commission (the "SEC") subsequent to the date we filed the 2024 10-K with the SEC. You should not place undue reliance on any forward-looking statements. Further, any forward-looking statement in this report speaks only as of the date hereof, unless it is specifically otherwise stated to be made as of a different date. Except as required by law, we undertake no obligation to update, and expressly disclaim any duty to update, our forward-looking statements, whether as a result of circumstances or events that arise after the date hereof, new information, or otherwise.
Trademarks
Solely for convenience, our trademarks and trade names in this report are referred to without the ® and ™ symbols, but such references should not be construed as any indicator that we will not assert, to the fullest extent under applicable law, our rights thereto.
3
PART I. F
INANCIAL INFORMATION
I
tem 1. Financial Statements
ORTHOFIX MEDICAL INC.
C
ondensed Consolidated Balance Sheets
(U.S. Dollars, in thousands, except par value data)
June 30,
2025
December 31,
2024
(Unaudited)
Assets
Current assets
Cash and cash equivalents
$
65,606
$
83,238
Restricted cash
3,083
2,500
Accounts receivable, net of allowances of $
8,909
and $
7,418
, respectively
129,556
134,713
Inventories
172,993
189,452
Prepaid expenses and other current assets
24,592
23,382
Total current assets
395,830
433,285
Property, plant, and equipment, net
129,200
139,804
Intangible assets, net
78,868
98,803
Goodwill
194,934
194,934
Other long-term assets
38,325
26,468
Total assets
$
837,157
$
893,294
Liabilities and shareholders’ equity
Current liabilities
Accounts payable
$
45,098
$
48,803
Current portion of finance lease liability
797
755
Other current liabilities
102,486
119,070
Total current liabilities
148,381
168,628
Long-term debt
157,047
157,015
Long-term portion of finance lease liability
17,448
17,835
Other long-term liabilities
55,934
46,692
Total liabilities
378,810
390,170
Contingencies (Note 7)
Shareholders’ equity
Common shares $
0.10
par value;
100,000
shares authorized;
39,483
and
38,486
issued and outstanding as of June 30,
2025, and December 31, 2024, respectively
3,948
3,849
Additional paid-in capital
796,807
779,718
Accumulated deficit
(
343,316
)
(
276,141
)
Accumulated other comprehensive income (loss)
908
(
4,302
)
Total shareholders’ equity
458,347
503,124
Total liabilities and shareholders’ equity
$
837,157
$
893,294
The accompanying notes form an integral part of these condensed consolidated financial statements.
4
ORTHOFIX MEDICAL INC.
C
ondensed Consolidated Statements of Operations and Comprehensive Loss
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands, except per share data)
2025
2024
2025
2024
Net sales
$
203,121
$
198,620
$
396,767
$
387,228
Cost of sales
63,588
63,871
135,615
125,237
Gross profit
139,533
134,749
261,152
261,991
Sales, general, and administrative
136,493
134,218
269,474
265,909
Research and development
15,934
18,049
35,700
37,541
Acquisition-related amortization, impairment, and remeasurement (Note 11)
3,109
7,388
20,854
12,784
Operating loss
(
16,003
)
(
24,906
)
(
64,876
)
(
54,243
)
Interest expense, net
(
3,950
)
(
4,943
)
(
8,456
)
(
9,501
)
Other income (expense), net
5,730
(
2,510
)
6,976
(
3,784
)
Loss before income taxes
(
14,223
)
(
32,359
)
(
66,356
)
(
67,528
)
Income tax benefit (expense)
142
(
1,084
)
(
819
)
(
1,935
)
Net loss
$
(
14,081
)
$
(
33,443
)
$
(
67,175
)
$
(
69,463
)
Net loss per common share:
Basic
$
(
0.36
)
$
(
0.88
)
$
(
1.71
)
$
(
1.84
)
Diluted
(
0.36
)
(
0.88
)
(
1.71
)
(
1.84
)
Weighted average number of common shares:
Basic
39,501
38,020
39,317
37,787
Diluted
39,501
38,020
39,317
37,787
Other comprehensive income (loss), before tax
Unrealized gain on debt securities
—
—
—
1,671
Reclassification adjustment for historical unrealized gain on debt security
—
(
1,671
)
—
(
1,671
)
Currency translation adjustment
3,464
(
400
)
5,210
(
1,438
)
Other comprehensive income (loss), before tax
3,464
(
2,071
)
5,210
(
1,438
)
Income tax expense related to other comprehensive income (loss)
—
—
—
—
Other comprehensive income (loss), net of tax
3,464
(
2,071
)
5,210
(
1,438
)
Comprehensive loss
$
(
10,617
)
$
(
35,514
)
$
(
61,965
)
$
(
70,901
)
The accompanying notes form an integral part of these condensed consolidated financial statements.
5
ORTHOFIX MEDICAL INC.
Condensed Consolidated Statements of Changes in Shareholders' Equity
(Unaudited, U.S. Dollars, in thousands)
Number of
Common
Shares
Outstanding
Common
Shares
Additional
Paid-in
Capital
Accumulated Deficit
Accumulated
Other
Comprehensive Income (Loss)
Total
Shareholders’
Equity
At December 31, 2024
38,486
$
3,849
$
779,718
$
(
276,141
)
$
(
4,302
)
$
503,124
Net loss
—
—
—
(
53,094
)
—
(
53,094
)
Other comprehensive income, net of tax
—
—
—
—
1,746
1,746
Share-based compensation expense
—
—
6,469
—
—
6,469
Common shares issued, net
610
61
(
12
)
—
—
49
At March 31, 2025
39,096
$
3,910
$
786,175
$
(
329,235
)
$
(
2,556
)
$
458,294
Net loss
—
—
—
(
14,081
)
—
(
14,081
)
Other comprehensive income, net of tax
—
—
—
—
3,464
3,464
Share-based compensation expense
—
—
7,824
—
—
7,824
Common shares issued, net
387
38
2,808
—
—
2,846
At June 30, 2025
39,483
$
3,948
$
796,807
$
(
343,316
)
$
908
$
458,347
(Unaudited, U.S. Dollars, in thousands)
Number of
Common
Shares
Outstanding
Common
Shares
Additional
Paid-in
Capital
Accumulated Deficit
Accumulated
Other
Comprehensive Income
(Loss)
Total
Shareholders’
Equity
At December 31, 2023
37,165
$
3,717
$
746,450
$
(
150,144
)
(
1,293
)
$
598,730
Net loss
—
—
—
(
36,020
)
—
(
36,020
)
Other comprehensive income, net of tax
—
—
—
—
633
633
Share-based compensation expense
—
—
8,800
—
—
8,800
Common shares issued, net
245
24
(
1,852
)
—
—
(
1,828
)
At March 31, 2024
37,410
$
3,741
$
753,398
$
(
186,164
)
$
(
660
)
$
570,315
Net loss
—
—
—
(
33,443
)
—
(
33,443
)
Other comprehensive loss, net of tax
—
—
—
—
(
2,071
)
(
2,071
)
Share-based compensation expense
—
—
9,959
—
—
9,959
Common shares issued, net
629
63
1,181
—
—
1,244
At June 30, 2024
38,039
$
3,804
$
764,538
$
(
219,607
)
$
(
2,731
)
$
546,004
The accompanying notes form an integral part of these condensed consolidated financial statements.
6
ORTHOFIX MEDICAL INC.
C
ondensed Consolidated Statements of Cash Flows
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Cash flows from operating activities
Net loss
$
(
67,175
)
$
(
69,463
)
Adjustments to reconcile net loss to net cash from operating activities
Depreciation, amortization, and impairment
51,302
28,894
Inventory reserve expenses
25,393
13,759
Amortization of inventory fair value step-up
—
6,094
Amortization of operating lease assets, debt costs, and other assets
2,377
2,986
Provision for expected credit losses
1,837
1,573
Deferred income taxes
12
1,180
Share-based compensation expense
14,293
18,759
Loss on disposal of fixed assets
581
2,566
Change in valuation of investment securities
(
31
)
3,992
Change in fair value of contingent consideration
(
1,373
)
4,240
Other
(
1,188
)
2,297
Changes in operating assets and liabilities
Accounts receivable
5,089
710
Inventories
(
5,890
)
(
8,571
)
Prepaid expenses and other current assets
(
394
)
2,717
Accounts payable
(
9,138
)
(
7,501
)
Other current liabilities
(
21,763
)
(
9,977
)
Other long-term assets and liabilities
(
684
)
(
3,866
)
Net cash used in operating activities
(
6,752
)
(
9,611
)
Cash flows from investing activities
Capital expenditures
(
13,845
)
(
20,533
)
Other investing activities
12
(
50
)
Net cash used in investing activities
(
13,833
)
(
20,583
)
Cash flows from financing activities
Proceeds from issuance of common shares
3,054
3,191
Payments related to tax withholdings for share-based compensation
(
159
)
(
3,775
)
Payments related to finance lease obligation
(
375
)
(
346
)
Proceeds from credit facility
—
40,000
Repayment of borrowings from credit facility
—
(
15,000
)
Payment of debt issuance costs and other financing activities
(
531
)
(
2,392
)
Net cash provided by financing activities
1,989
21,678
Effect of exchange rate changes on cash
1,547
(
375
)
Net change in cash and cash equivalents
(
17,049
)
(
8,891
)
Cash, cash equivalents, and restricted cash at the beginning of period
85,738
37,757
Cash, cash equivalents, and restricted cash at the end of period
$
68,689
$
28,866
Components of cash, cash equivalents, and restricted cash at the end of period
Cash and cash equivalents
$
65,606
$
26,366
Restricted cash
3,083
2,500
Cash, cash equivalents, and restricted cash at the end of period
$
68,689
$
28,866
Noncash investing activities - Accrued purchases of capital expenditures
$
10,990
$
5,996
Noncash investing activities - Purchase of intangible assets
40
50
The accompanying notes form an integral part of these condensed consolidated financial statements.
7
ORTHOFIX MEDICAL INC.
N
otes to the Unaudited Condensed Consolidated Financial Statements
1. Business and basis of presentation
Description of the Business
Orthofix Medical Inc. (the "Company" or "Orthofix") is a global medical technology company headquartered in Lewisville, Texas. By providing medical technologies that heal musculoskeletal pathologies, the Company delivers exceptional experiences and life-changing solutions to patients around the world. Orthofix offers a comprehensive portfolio of spinal hardware, bone growth therapies, specialized orthopedic solutions, biologics, and enabling technologies, including the 7D FLASH navigation system.
Basis of Presentation
The accompanying unaudited condensed consolidated financial statements have been prepared in accordance with generally accepted accounting principles in the United States ("U.S. GAAP") for interim financial information and with the instructions to Form 10-Q and Rule 10-01 of Regulation S-X. Pursuant to these rules and regulations, certain information and note disclosures normally included in financial statements prepared in accordance with U.S. GAAP have been condensed or omitted. In the opinion of management, all adjustments (consisting of normal recurring items) considered necessary for a fair statement have been included. These condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and related notes contained in the Company's 2024 Form 10-K. Operating results for the three and six months ended June 30, 2025, are not necessarily indicative of the results that may be expected for other interim periods or the year ending December 31, 2025.
The preparation of financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the amounts reported in the financial statements and accompanying notes. On an ongoing basis, the Company evaluates its estimates, including those related to revenue recognition; contractual allowances; allowances for expected credit losses; inventories; valuation of intangible assets; goodwill; fair value measurements, including contingent consideration; litigation and contingent liabilities; tax matters; and share-based compensation. Actual results could differ from these estimates.
Changes in Presentation of Consolidated Financial Statements
Certain prior year balances have been reclassified in the condensed consolidated financial statements to conform to current period presentation.
2. Recently adopted accounting standards and recently issued accounting pronouncements
Adoption of Accounting Standards Update ("ASU") 2023-09 - Improvements to Income Tax Disclosures
In December 2023, the Financial Accounting Standards Board ("FASB") issued ASU 2023-09, which enhances the transparency and usefulness of income tax disclosures required pursuant to Topic 740,
Income Taxes
, to provide information to better assess how an entity's operations, tax risks and tax planning, and operational opportunities affect its tax rate and future cash flows. The Company adopted this standard effective January 1, 2025, on a modified retrospective basis. Adoption of this standard did not have a material impact on the Company's consolidated balance sheet, statements of operations, or cash flows.
8
Recently Issued Accounting Pronouncements
Topic
Description of Guidance
Effective Date
Status of Company's Evaluation
Disclosure Improvements - Codification Amendments in Response to the SEC's Disclosure Update and Simplification Initiative (ASU 2023-06)
Adds interim and annual disclosure requirements to a variety of subtopics in the Accounting Standards Codification, including those focusing on accounting changes, earnings per share, debt, and repurchase agreements. The guidance will be applied prospectively. The effective date will be the date when the SEC's removal of the related disclosure requirement becomes effective, with early adoption prohibited.
Various
The Company is currently evaluating the impact this ASU may have on its consolidated financial statements.
Disaggregation of Income Statement Expenses (ASU 2024-03)
Improve financial reporting by requiring that public business entities disclose additional information about specific expense categories in the note to the financial statements at interim and annual reporting periods. The amendments are to be applied prospectively to financial statements issued for reporting periods after the effective date or retrospectively to all prior periods presented in the financial statements.
January 1, 2027
The Company is currently evaluating the impact this ASU may have on its consolidated financial statements.
Other recently issued ASUs, excluding those ASUs which have already been disclosed as adopted or described above, were assessed and determined not applicable, or are expected to have minimal impact on the Company's condensed consolidated financial statements.
3. Inventories
Inventories were as follows:
(U.S. Dollars, in thousands)
June 30,
2025
December 31,
2024
(Unaudited)
Raw materials
$
26,588
$
27,180
Work-in-process
61,408
56,920
Finished products
84,997
105,352
Inventories
$
172,993
$
189,452
9
4. Leases
A summary of the Company's lease portfolio as of
June 30, 2025, and December 31, 2024, is presented in the table below:
(U.S. Dollars, in thousands)
Classification
June 30,
2025
December 31,
2024
(Unaudited)
Assets
Operating leases
Other long-term assets
$
24,859
$
17,238
Finance leases
Property, plant, and equipment, net
14,908
15,386
Total lease assets
$
39,767
$
32,624
Liabilities
Current
Operating leases
Other current liabilities
$
3,048
$
4,023
Finance leases
Current portion of finance lease liability
797
755
Long-term
Operating leases
Other long-term liabilities
26,398
14,084
Finance leases
Long-term portion of finance lease liability
17,448
17,835
Total lease liabilities
$
47,691
$
36,697
Supplemental cash flow information related to leases was as follows:
(Unaudited, U.S. Dollars, in thousands)
Six Months Ended
June 30, 2025
Six Months Ended
June 30, 2024
Cash paid for amounts included in the measurement of lease liabilities
Operating cash flows from operating leases
$
4,407
$
4,311
Operating cash flows from finance leases
401
417
Financing cash flows from finance leases
375
346
ROU assets obtained in exchange for lease obligations
Operating leases
11,690
721
Finance leases
28
—
5. Long-term debt
The carrying values of the Company's outstanding debt obligations as of
June 30, 2025, and December 31, 2024, were as follows:
(U.S. Dollars, in thousands)
June 30,
2025
December 31,
2024
(Unaudited)
Outstanding Term Loans
Principal amount
$
160,000
$
160,000
Unamortized original debt discount
(
2,083
)
(
2,327
)
Unamortized debt issuance costs and lenders fees
(
870
)
(
658
)
Total indebtedness from outstanding term loans
157,047
157,015
Revolving Credit Facilities
Principal amount outstanding
—
—
Total indebtedness outstanding
$
157,047
$
157,015
Current portion of long-term debt
$
—
$
—
Long-term debt
157,047
157,015
Total indebtedness outstanding
$
157,047
$
157,015
10
On November 7, 2024, the Company, as borrower, and its U.S. subsidiaries entered into a $
275.0
million secured credit agreement (the "Credit Agreement") with Oxford Finance LLC, as administrative agent and as collateral agent ("Oxford") and certain lenders party thereto, including Oxford, K2 HealthVentures LLC, and HSBC Ventures USA Inc. The Credit Agreement contains financial covenants requiring the Company to maintain (i) a minimum level of liquidity at all times and (ii) a maximum total debt-to-EBITDA leverage ratio (measured on a quarterly basis) during the term of the facility
. As of June 30, 2025, the Company was in compliance with all required financial covenants.
As of June 30, 2025
, the Company had
no
borrowings on its available lines of credit in Italy, which provide up to an aggregate amount of €
5.5
million ($
6.5
million).
6. Fair value measurements and investments
The fair value measurements of the Company's financial assets and liabilities measured on a recurring basis were as follows:
June 30,
2025
December 31,
2024
(U.S. Dollars, in thousands)
Level 1
Level 2
Level 3
Total
Total
(Unaudited)
Assets
Neo Medical convertible loan agreement
$
—
$
—
$
—
$
—
$
—
Neo Medical preferred equity securities
—
—
—
—
—
Total
$
—
$
—
$
—
$
—
$
—
Liabilities
Lattus contingent consideration
$
—
$
—
$
(
14,027
)
$
(
14,027
)
$
(
15,400
)
Deferred compensation plan
—
(
1,695
)
—
(
1,695
)
(
1,703
)
Total
$
—
$
(
1,695
)
$
(
14,027
)
$
(
15,722
)
$
(
17,103
)
Neo Medical Convertible Loan Agreement and Equity Investment
On October 1, 2020, the Company purchased shares of Neo Medical's preferred stock for consideration of $
5.0
million and entered into a Convertible Loan Agreement (the "Convertible Loan") pursuant to which Orthofix loaned Neo Medical CHF
4.6
million, or $
5.0
million at the date of issuance. In April 2024, the Company converted the Convertible Loan into shares of Neo Medical preferred equity securities. On November 14, 2024, the Company sold and transferred all shares of Neo Medical's preferred equity securities for CHF
6.6
million, or $
7.4
million.
The table below presents a reconciliation of the beginning and ending balances of the Company's investment in Neo Medical preferred equity securities:
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Fair value of Neo Medical preferred equity securities at January 1
$
—
$
4,951
Conversion of loan into preferred equity securities
—
8,224
Unrealized loss recognized in other expense, net
—
(
2,233
)
Fair value of Neo Medical preferred equity securities at June 30
$
—
$
10,942
Cumulative unrealized loss on Neo Medical preferred equity securities
$
—
$
(
2,953
)
11
The following table provides a reconciliation of the beginning and ending balances of the Convertible Loan, which was measured at fair value using significant unobservable inputs:
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Fair value of Neo Medical Convertible Loan at January 1
$
—
$
6,760
Gain recognized in other comprehensive income
—
1,671
Interest recognized in interest income, net
—
162
Foreign currency remeasurement recognized in other expense, net
—
(
602
)
Expected credit loss recognized in other income, net
—
260
Conversion into preferred equity securities
—
(
8,224
)
Realized foreign currency loss recognized in other expense, net
—
(
27
)
Fair value of Neo Medical Convertible Loan at June 30
$
—
$
—
Contractual value of Neo Medical Convertible Loan at June 30
$
—
$
—
Allowance for credit loss recognized in other income (expense), net
—
—
Amortized cost basis of Neo Medical Convertible Loan at June 30
$
—
$
—
Lattus Contingent Consideration
In connection with the merger with SeaSpine Holdings Corporation ("SeaSpine") in 2023 (the "SeaSpine Merger"), the Company assumed a contingent consideration obligation under a purchase agreement between SeaSpine and Lattus Spine LLC ("Lattus") executed in December 2022. Under the terms of this agreement, the Company may be required to make installment payments to Lattus (the "Lattus Contingent Consideration") at certain dates based on future net sales of certain products (the "Lateral Products").
The estimated fair value of the Lattus Contingent Consideration is determined using a Monte Carlo simulation and a discounted cash flow model requiring significant inputs which are not observable in the market. The significant inputs include assumptions related to the timing and probability of launch dates for the Lateral Products, estimated future sales of the Lateral Products, revenue risk-adjusted discount rate, revenue volatility, and discount rates matched to the timing of payments. The following table provides a reconciliation of the beginning and ending balances for the Lattus Contingent Consideration measured at estimated fair value using significant unobservable inputs (Level 3):
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Lattus Contingent Consideration estimated fair value at January 1
$
15,400
$
8,500
Change in fair value recognized in acquisition-related amortization, impairment, and remeasurement
(
1,373
)
4,240
Lattus Contingent Consideration estimated fair value at June 30
$
14,027
$
12,740
The estimated fair value of the Lattus Contingent Consideration as of June 30, 2025, was
$
14.0
million; however, the actual amount ultimately paid could be higher or lower this. As of June 30, 2025
, the Company classified the remaining Lattus Contingent Consideration liability of $
10.5
million and $
3.5
million within other current liabilities and other long-term liabilities, respectively.
The following table provides quantitative information related to certain key assumptions utilized within the valuation as of
June 30, 2025:
(Unaudited, U.S. Dollars, in thousands)
Fair Value as of
June 30, 2025
Unobservable inputs
Estimate
Lattus Contingent Consideration
$
14,027
Counterparty discount rates
10.8
% -
11.0
%
Revenue risk-adjusted discount rates
6.4
% -
6.8
%
12
7. Commitments and Contingencies
Arbitration claims with former executives
In September 2023, the Company's Board of Directors (the "Board") terminated the employment of Keith Valentine, John Bostjancic, and Patrick Keran, who had served respectively as the Company's President and Chief Executive Officer, Chief Financial Officer, and Chief Legal Officer. The Board's decision followed an investigation conducted by independent outside legal counsel and directed and overseen by the Company's independent directors. As a result of the investigation, the Board determined that each of these executives engaged in repeated inappropriate and offensive conduct that violated multiple code of conduct requirements and was inconsistent with the Company's values and culture. The Company notified each of Messrs. Valentine, Bostjancic, and Keran that their respective terminations were being made for "Cause," as defined in applicable employment-related agreements (including each executive's respective Change in Control and Severance Agreement, dated June 19, 2023). The Company also notified each of Messrs. Valentine, Bostjancic, and Keran that it did not believe it was required to make any further payments to them, other than payment of salary through September 12, 2023. The Board also requested that Mr. Valentine resign as a director, which he did in October 2023.
In January 2024, the Company received written notices of arbitration claims from counsel to Messrs. Valentine, Bostjancic, and Keran. Each of the arbitration claims asserts that the respective former executive was wrongfully terminated for "Cause" because the former executive's conduct did not meet the contractually applicable definition of "Cause." The claims seek relief for, among other things, alleged breach of contract, defamation, false light invasion of privacy, deceit, as well as indemnification and advancement for attorneys' fees. The three former executives seek severance payments, as well as the value of forfeited equity grants under applicable change in control and severance agreements and further damages as a result of purported defamatory statements. In addition, in September 2024, Messrs. Valentine, Bostjancic and Keran filed an action in California State Court against former director and interim CEO Catherine Burzik and current director Wayne Burris, seeking relief for, among other things, alleged defamation, false light invasion of privacy, intentional misrepresentation, false promise, and tortious interference with contract.
The Company disagrees with the allegations contained in the arbitration demands and in the action against Ms. Burzik and Mr. Burris and is vigorously defending the asserted claims. Due in part to the preliminary nature of this matter, the Company currently cannot reasonably estimate a possible loss, or range of loss, that may arise from these claims.
Securities class action complaints
On August 21, 2024, a securities class action complaint captioned
Bernal v. Orthofix Medical Inc., et al.
, Case No. 24-cv-00690, was filed in the United States District Court for the Eastern District of Texas (the "Bernal Complaint"). The plaintiff, a purported Company shareholder, alleges through the complaint violations of Sections 10(b) and 20(a) of the Exchange Act, and SEC Rule 10b-5 promulgated thereunder, and names as defendants the Company and the following former Company directors and officers: Jon Serbousek (former director and former President and Chief Executive Officer), Keith Valentine (former director and former President and Chief Executive Officer), John Bostjancic (former Chief Financial Officer), and Patrick Keran (former Chief Legal Officer). The complaint alleges that the Company made, and the named former directors and officers caused the Company to make, materially false and misleading statements between October 11, 2022, and September 12, 2023, that, according to the complaint, falsely assured the market regarding Messrs. Valentine, Bostjancic, and Keran's respective commitments to, among other things, ethical and legal standards and corporate responsibility.
On September 6, 2024, a securities class action complaint captioned
O'Hara v. Orthofix Medical Inc., et al.
, Case No. 24-cv-01593, was filed in the United States District Court for the Southern District of California (the "O'Hara Complaint"). The plaintiff, a purported former shareholder of SeaSpine at the time of the SeaSpine Merger, alleges through the complaint violations of Sections 11, 12 and 15 of the Securities Act, and names most of the same defendants as the Bernal Complaint, as well as certain additional current and/or former Company directors and officers. The complaint makes similar assertions to the Bernal complaint, and alleges that the Company's registration statement on Form S-4 filed in 2022 in connection with the SeaSpine Merger, as well as related written and oral offering materials, contained untrue statements of material fact and material omissions, including, among other things, with respect to the effectiveness of the Company's internal controls. On November 26, 2024, the O'Hara Complaint was transferred to the Eastern District of Texas, and on December 11, 2024, the O'Hara Complaint was consolidated with the Bernal Complaint. On April 17, 2025, the plaintiffs filed an amended complaint in the consolidated action, captioned
In re Orthofix Medical Inc. Securities Litigation
, with substantially the same allegations contained in the Bernal Complaint and the O'Hara Complaint. The consolidated case is captioned
In re Orthofix Medical Inc. Securities Litigation
, Case No. 24-cv-00690 and is pending in the Eastern District of Texas. The Company and the individual defendants moved to dismiss the amended complaint on May 15, 2025.
On October 28, 2024, a derivative shareholder complaint was filed against certain of the Company's current and former officers and directors alleging derivative liability for the allegations made in the two complaints noted above. On December 18, 2024, a second
13
derivative shareholder complaint was filed with the same allegations made in the first derivative shareholder complaint. On March 21, 2025, the two derivative shareholder complaints were consolidated into one case.
The Company disagrees with the legal claims asserted in these complaints and is vigorously defending them. Due in part to the preliminary nature of these three matters, the Company currently cannot reasonably estimate a possible loss, or range of loss, that may arise from the respective complaints.
Commitments
As a result of the SeaSpine Merger, the Company became party to agreements with certain distributor partners that provide the Company with an option to purchase, and an option for those partners to require the Company to purchase, the distribution business of those partners at specified future dates. At such time, the Company or distributor may (in certain cases, subject to satisfying certain conditions) submit written notice to the other of its intention to exercise its rights and initiate or require the purchase. Upon receipt of the written notice, the Company and the distributor will work in good faith to consummate the purchase, provided that the distributor meets the required conditions of such purchase option. Under certain of these agreements, the purchase price would be paid in shares of the Company's common stock, whereas for others, the purchase price can be paid in cash or shares, at the Company's option. Based on the closing price of the Company's common stock as of June 30, 2025
, assuming the options under all the relevant agreements were exercised, the estimated total number of shares the Company would issue under these agreements was approximately
0.4
million shares for agreements that must be settled in shares of the Company's stock. The Company has received notification from one such distributor, who has notified the Company of its decision to exercise its buyout option. The Company is currently in negotiations with this distributor in regard to the consummation of the potential acquisition, which is subject to the distributor satisfying certain conditions.
Italian Medical Device Payback ("IMDP")
In 2015, the Italian Parliament introduced rules for entities that supply goods and services to the Italian National Healthcare System. A key provision of the law is a 'payback' measure, requiring medical device companies in Italy to make payments to the Italian government if medical device expenditures exceed regional maximum ceilings. Companies are required to make payments equal to a percentage of expenditures exceeding maximum regional caps.
In the third quarter of 2022, the Italian Ministry of Health provided guidelines to the Italian regions and provinces on seeking payback of expenditure overruns relating to the 2015 through 2018 calendar years. Since receiving the guidelines, several regions and provinces have requested payment from affected medical device companies, including the Company. The Company has taken legal action to dispute the legality of such measures. In July 2024, the Italian Constitutional Court issued two judgments following public hearings on the matter held in May 2024. These judgments (i) declared the payback system itself as constitutionally legitimate and (ii) extended previously communicated reductions in the payback liability for certain fiscal years to all medical device companies, regardless of whether or not they had waived their legal claims on the matter.
The Company accounts for the estimated cost of the IMDP as sales, general, and administrative expense and periodically reassesses the liability based upon current facts and circumstances. As a result, the Company recorded expenses of $
0.3
million and $
0.6
million for the
three and six months ended June 30, 2025
, respectively, and expenses of $
0.3
million and $
0.6
million for the
three and six months ended June 30, 2024, respectively. As of June 30, 2025
, the Company has accrued $
10.0
million related to the IMDP, which it has classified within other long-term liabilities; however, the actual liability could be higher or lower than the amount accrued once all legal proceedings are resolved and upon further clarification of the IMDP by the Italian authorities for more recent fiscal years.
8. Accumulated other comprehensive income (loss)
The components of and changes in accumulated other comprehensive income (loss) were as follows:
(Unaudited, U.S. Dollars, in thousands)
Currency
Translation
Adjustments
Neo Medical Convertible Loan
Accumulated Other
Comprehensive Income (Loss)
Balance at December 31, 2024
$
(
4,074
)
$
(
228
)
$
(
4,302
)
Other comprehensive income
5,210
—
5,210
Income taxes
—
—
—
Balance at June 30, 2025
$
1,136
$
(
228
)
$
908
14
9. Revenue recognition and accounts receivable
Revenue Recognition
The Company has two reporting segments: Global Spine and Global Orthopedics. Within the Global Spine reporting segment, there are two product categories: (i) Bone Growth Therapies, and (ii) Spinal Implants, Biologics, and Enabling Technologies.
The tables below present net sales by product category by reporting segment:
Three Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Change
Bone Growth Therapies
$
62,573
$
59,135
5.8
%
Spinal Implants, Biologics, and Enabling Technologies
107,251
108,899
-
1.5
%
Global Spine
169,824
168,034
1.1
%
Global Orthopedics
33,297
30,586
8.9
%
Net sales
$
203,121
$
198,620
2.3
%
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Change
Bone Growth Therapies
$
117,623
$
111,612
5.4
%
Spinal Implants, Biologics, and Enabling Technologies
216,037
217,715
-
0.8
%
Global Spine
333,660
329,327
1.3
%
Global Orthopedics
63,107
57,901
9.0
%
Net sales
$
396,767
$
387,228
2.5
%
Product Sales and Marketing Service Fees
The table below presents product sales and marketing service fees, which are both components of net sales:
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Product sales
$
191,395
$
185,417
$
373,028
$
361,248
Marketing service fees
11,726
13,203
23,739
25,980
Net sales
$
203,121
$
198,620
$
396,767
$
387,228
Product sales primarily consist of the sale of bone growth therapies devices, spinal implants, certain biologics, enabling technologies, and orthopedics products. Marketing service fees are received from MTF Biologics ("MTF") based on total sales of biologics tissues sourced from MTF and relate solely to the Global Spine reporting segment. The Company partners with MTF to provide certain allograft solutions for various spine, orthopedic and other bone repair needs, with this partnership allowing the Company to exclusively market certain biologic offerings.
Accounts receivable and related allowances
The following table provides a detail of changes in the Company's allowance for expected credit losses for the
three and six months ended June 30, 2025 and 2024:
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Allowance for expected credit losses beginning balance
$
8,602
$
8,398
$
7,418
$
7,130
Current period provision for expected credit losses
779
197
1,837
1,573
Write-offs charged against the allowance and other
(
747
)
(
184
)
(
758
)
(
203
)
Effect of changes in foreign exchange rates
275
(
43
)
412
(
132
)
Allowance for expected credit losses ending balance
$
8,909
$
8,368
$
8,909
$
8,368
15
10. Business segment information
The Company's operations are managed through
two
reporting segments: Global Spine and Global Orthopedics. These reporting segments represent the operating segments for which the
President and Chief Executive Officer
, who is also the Chief Operating Decision Maker ("CODM"), reviews financial information and makes resource allocation decisions among businesses.
The primary metric used by the CODM in managing the Company is adjusted earnings before interest, tax, depreciation, and amortization ("adjusted EBITDA", a non-GAAP financial measure). Adjusted EBITDA represents earnings before interest income (expense), income taxes, depreciation, and amortization, and excludes the impact of share-based compensation, gains and losses related to changes in foreign exchange rates, charges related to the SeaSpine Merger and other strategic investments, restructuring costs and impairments related to M6 product lines, acquisition-related fair value adjustments, gains and/or losses on investments, litigation and investigation charges, succession charges, and refunds associated with the employee retention credit established by the Coronavirus Aid, Relief, and Economic Security Act.
Corporate activities are comprised of operating expenses not directly identifiable within the two reporting segments, such as human resources, finance, legal, and information technology functions. The Company neither discretely allocates assets, other than goodwill, to its operating segments nor evaluates the operating segments using discrete asset information.
Global Spine
The Global Spine reporting segment offers two primary product categories: (i) Bone Growth Therapies and (ii) Spinal Implants, Biologics, and Enabling Technologies.
The Bone Growth Therapies product category manufactures, distributes, sells, and provides support services for market-leading bone growth stimulation devices that enhance bone fusion. These Class III medical devices are indicated as an adjunctive, noninvasive treatment to improve fusion success rates in the cervical and lumbar spine as well as a therapeutic treatment for non-spinal, appendicular fractures, treating both fresh or nonunion fractures. These products are sold almost exclusively in the U.S., using distributors and direct sales representatives to provide our devices to healthcare providers and their patients.
Spinal Implants, Biologics, and Enabling Technologies comprises (i) a broad portfolio of spine fixation implant products used in surgical procedures of the spine, (ii) one of the most comprehensive biologics portfolios in both the demineralized bone matrix and cellular allograft market segments, and (iii) image-guided surgical solutions to facilitate degenerative, minimally invasive, and complex surgical procedures. Spinal Implants, Biologics, and Enabling Technologies products are sold through a network of distributors and sales representatives to hospitals and healthcare providers on a global basis for Spinal Implants and Enabling Technologies, and primarily within the U.S. for Biologics.
Global Orthopedics
The Global Orthopedics reporting segment offers products and solutions for the underserved limb reconstruction market that encompasses four pillars: deformity correction, limb lengthening, complex fracture management, and limb preservation. This reporting segment specializes in the design, development, and marketing of external and internal fixation orthopedic products that are coupled with enabling digital technologies to serve the complete patient treatment pathway. The Company sells these products worldwide through a global network of distributors and sales representatives to hospitals, healthcare organizations, and healthcare providers.
16
The following table presents adjusted EBITDA, the primary metric used in managing the Company, by reporting segment:
Three Months Ended June 30, 2025
Six Months Ended June 30, 2025
(U.S. Dollars, in thousands)
Global Spine
Global Orthopedics
Total
Global Spine
Global Orthopedics
Total
Segment revenues
$
169,824
$
33,297
$
203,121
$
333,660
$
63,107
$
396,767
Less:
Non-GAAP Cost of sales
42,811
12,266
55,077
87,398
24,137
111,535
Non-GAAP Sales, general, and administrative
97,169
17,990
115,159
189,708
35,911
225,619
Non-GAAP Research and development
11,761
2,674
14,435
23,384
5,526
28,910
Other segment expenses (benefits)
2,464
6
2,470
6,907
(
169
)
6,738
Add:
Non-GAAP Depreciation, amortization, and share-based compensation expense
10,814
2,124
12,938
19,686
4,756
24,442
Segment Adjusted EBITDA
$
26,433
$
2,485
$
28,918
$
45,949
$
2,458
$
48,407
Reconciling items:
Corporate operating expenses
8,273
16,331
Interest expense, net
3,950
8,456
Depreciation and amortization
16,871
51,302
Share-based compensation expense
7,824
14,293
Foreign exchange impact
(
2,751
)
(
3,795
)
SeaSpine merger-related costs
4,886
6,016
Restructuring costs and impairments related to M6 product lines
3,354
15,480
Strategic investments
353
3,867
Acquisition-related fair value adjustments
(
763
)
(
1,373
)
Interest and loss on investments
(
31
)
(
31
)
Litigation and investigation costs
4,029
7,071
Employee retention credit
(
2,854
)
(
2,854
)
Loss before income taxes
$
(
14,223
)
$
(
66,356
)
17
Three Months Ended June 30, 2024
Six Months Ended June 30, 2024
(U.S. Dollars, in thousands)
Global Spine
Global Orthopedics
Total
Global Spine
Global Orthopedics
Total
Segment Revenues
$
168,034
$
30,586
$
198,620
$
329,327
$
57,901
$
387,228
Less:
Non-GAAP Cost of sales
43,958
12,469
56,427
88,812
23,316
112,128
Non-GAAP Sales, general, and administrative
92,542
19,375
111,917
184,354
37,522
221,876
Non-GAAP Research and development
14,118
3,542
17,660
30,063
6,854
36,917
Other segment expenses (benefits)
(
170
)
36
(
134
)
(
137
)
(
72
)
(
209
)
Add:
Non-GAAP Depreciation, amortization, and share-based compensation expense
10,102
5,015
15,117
21,343
8,406
29,749
Segment Adjusted EBITDA
$
27,688
$
179
$
27,867
$
47,578
$
(
1,313
)
$
46,265
Reconciling items:
Corporate operating expenses
11,234
21,967
Interest expense, net
4,943
9,501
Depreciation and amortization
14,032
28,894
Share-based compensation expense
9,959
18,759
Foreign exchange impact
851
2,439
SeaSpine merger-related costs
5,897
10,376
Strategic investments
311
431
Acquisition-related fair value adjustments
6,117
10,334
Interest and loss on investments
1,813
1,553
Litigation and investigation costs
(
277
)
1,983
Succession charges
5,346
7,556
Loss before income taxes
$
(
32,359
)
$
(
67,528
)
The following table presents depreciation and amortization by reporting segment:
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Global Spine
$
14,851
$
11,044
$
46,753
$
22,973
Global Orthopedics
1,419
2,191
3,355
4,398
Corporate
601
797
1,194
1,523
Total
$
16,871
$
14,032
$
51,302
$
28,894
18
Geographical information
The table below presents net sales by geographic destination for each reporting segment and for the consolidated Company:
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Global Spine
U.S.
$
161,850
$
159,191
$
314,553
$
311,056
International
7,974
8,843
19,107
18,271
Total Global Spine
169,824
168,034
333,660
329,327
Global Orthopedics
U.S.
9,888
7,742
18,866
15,896
International
23,409
22,844
44,241
42,005
Total Global Orthopedics
33,297
30,586
63,107
57,901
Consolidated
U.S.
171,738
166,933
333,419
326,952
International
31,383
31,687
63,348
60,276
Net sales
$
203,121
$
198,620
$
396,767
$
387,228
The following data includes net sales by geographic area:
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
U.S.
$
171,738
$
166,933
$
333,419
$
326,952
Italy
5,646
5,257
10,699
10,259
France
3,184
3,510
5,809
6,026
United Kingdom
3,118
2,623
6,155
5,254
Germany
2,265
2,393
4,473
4,498
Brazil
988
1,708
2,123
3,236
Others
16,182
16,196
34,089
31,003
Net Sales
$
203,121
$
198,620
$
396,767
$
387,228
The following data includes property, plant, and equipment by geographic area:
(U.S. Dollars, in thousands)
June 30,
2025
December 31,
2024
(Unaudited)
U.S.
$
114,012
$
125,541
Italy
10,085
9,472
Germany
1,794
1,904
Others
3,309
2,887
Total
$
129,200
$
139,804
19
11. Acquisition-related amortization, impairment, and remeasurement
Acquisition-related amortization, impairment, and remeasurement consists of (i) amortization and impairment related to intangible assets acquired through business combinations or asset acquisitions and (ii) remeasurement of any related contingent consideration arrangements.
Components of acquisition-related amortization, impairment, and remeasurement are as follows:
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Amortization and impairment of acquired intangibles
$
3,872
$
4,318
$
22,227
$
8,544
Changes in fair value of contingent consideration
(
763
)
3,070
(
1,373
)
4,240
Total
$
3,109
$
7,388
$
20,854
$
12,784
12. Share-based compensation
Components of share-based compensation expense are as follows:
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Cost of sales
$
468
$
514
$
929
$
1,090
Sales, general, and administrative
6,915
8,883
12,564
16,098
Research and development
441
562
800
1,571
Total
$
7,824
$
9,959
$
14,293
$
18,759
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
2025
2024
Stock options
$
1,594
$
1,382
$
2,463
$
2,500
Market-based stock options
592
499
1,238
826
Time-based restricted stock awards and units
3,528
6,254
6,522
12,127
Market-based / performance-based restricted stock units
1,650
1,303
3,070
2,141
Stock purchase plan
460
521
1,000
1,165
Total
$
7,824
$
9,959
$
14,293
$
18,759
During the three months ended June 30, 2025, and 2024
, the Company issued
0.4
million and
0.6
million shares, respectively, of common stock related to stock purchase plan issuances, stock option exercises, and the vesting of restricted stock awards and units. During the
six months ended June 30, 2025, and 2024
, the Company issued
1.0
million and
0.9
million shares, respectively, of common stock related to stock purchase plan issuances, stock option exercises, and the vesting of restricted stock awards and units.
13. Income taxes
Generally, income tax provisions for interim periods are based on an estimated annual income tax rate, adjusted for discrete tax items, with any changes affecting the estimated annual effective tax rate recorded in the interim period in which the change occurs. Due to the impact of losses not benefited by the Company's U.S., Canadian and Italian operations, the Company determined the estimated annual effective tax rate method would not provide a reliable estimate of the Company's overall annual effective tax rate. As such, the Company has calculated the tax provision using the actual effective rate for the three and six months ended June 30, 2025. Due to the impact of temporary differences on the U.S. current tax liability without any deferred tax benefit, the actual effective rate may vary in future quarters.
For the three months ended June 30, 2025, and 2024, the effective tax rate was
1.0
%
and
(
3.3
%)
, respectively. For the six months ended June 30, 2025, and 2024, the effective tax rate was
(
1.2
%)
and
(
2.9
%)
, respectively. The primary factors affecting the Company's effective tax rate for the three and six months ended June 30, 2025
, were certain losses not benefited and tax amortization on certain acquired intangibles.
20
14. Earnings per share ("EPS")
For the three and six months ended June 30, 2025
, no adjustments were made to net income for purposes of calculating basic and diluted EPS.
The following is a reconciliation of the weighted average shares used in diluted EPS computations.
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited, In thousands)
2025
2024
2025
2024
Weighted average common shares-basic
39,501
38,020
39,317
37,787
Effect of dilutive securities
Unexercised stock options and stock purchase plan
—
—
—
—
Unvested restricted stock units
—
—
—
—
Weighted average common shares-diluted
39,501
38,020
39,317
37,787
There were
8.7
million and
7.1
million weighted average outstanding options, time-based restricted stock awards and units, performance-based stock units, and market-based stock units not included in the diluted EPS computation for the
three months ended June 30, 2025, and 2024
, respectively, and
8.4
million and
6.9
million weighted average outstanding options, time-based restricted stock awards and units, performance-based stock units, and market-based stock units not included in the diluted EPS computation for the
six months ended June 30, 2025, and 2024
, respectively, because inclusion of these awards was anti-dilutive, or, for performance-based stock units and market-based stock units, all necessary conditions had not been satisfied by the end of the respective period.
15. Discontinuation of M6 product lines
In February 2025, the Company announced its plan to discontinue its M6-C artificial cervical disc and M6-L artificial lumbar disc product lines (together, the "M6 artificial discs" or "M6 product lines") in order to allocate associated resources and investment to more profitable growth opportunities. In accordance with ASC 205, Presentation of Financial Statements, the Company determined that the discontinuation of the M6 artificial disc does not represent a strategic shift that will have a major effect on its consolidated financial results. Therefore, any related financial results were not reported as discontinued operations. Although the M6 product lines did not meet the criteria to be considered a discontinued operation, these assets were determined to meet the criteria to be classified as held for sale as of March 31, 2025, as the Company expected to complete the sale of these assets before December 31, 2025.
During the second quarter of 2025, following several months of marketing and holding the M6 product lines for sale, the Company has determined that it is no longer probable that a sale of the M6 product lines will be completed within one year; therefore, the assets no longer qualify to be classified as held for sale. In accordance with this determination, all assets and liabilities associated with the M6 product lines have now been reclassified from held for sale to held and used. However, the Company has also fully impaired all assets associated with the M6 product lines as of June 30, 2025.
Financial results for the Company's M6 product lines continue to be presented within the Company's consolidated statements of operations and comprehensive loss.
A summary of impairment charges recognized during the
three and six months ended June 30, 2025, and the associated financial statement lines in which such costs are recognized is shown in the table below. All such changes are included within the Company's Global Spine reporting segment.
(Unaudited, U.S. Dollars, in thousands)
Financial Statement Line Item
Three Months Ended June 30, 2025
Six Months Ended June 30, 2025
Inventory reserve charges
Cost of sales
$
2,548
$
11,251
Impairment of property, plant, and equipment
Operating expenses
608
6,834
Impairment of developed technology intangible asset
Acquisition-related amortization, impairment, and remeasurement
—
14,097
Loss on M6 inventories and long-lived assets held for sale
$
3,156
$
32,182
21
16. Subsequent events
On July 4, 2025, the One Big Beautiful Bill Act (“OBBBA”) was signed into law, which includes a broad range of tax reform provisions affecting businesses. The OBBBA includes numerous changes to existing tax law including extending or making permanent certain business and international tax measures initially established under the 2017 Tax Cuts and Jobs Act, which were set to expire. Additionally, the OBBBA permanently eliminates the requirement to capitalize and amortize U.S. based research and experimental expenditures over five years, making these expenditures fully deductible in the period incurred and returns the interest limitation rules under Internal Revenue Code Section 163(j) to be calculated on tax basis EBITDA as opposed to earnings before interest and taxes (EBIT). The Company expects these provisions to impact deferred tax assets with a corresponding change in the U.S. valuation allowance. The Company will continue to analyze the OBBBA and its impact on its financial statements.
22
I
tem 2. Management's Discussion and Analysis of Financial Condition and Results of Operations
The following discussion and analysis of Orthofix Medical Inc.'s (sometimes referred to as "we," "us" or "our") financial condition and results of operations should be read in conjunction with the discussion under the heading "Forward-Looking Statements" and our condensed consolidated financial statements and related notes thereto appearing elsewhere in this Form 10-Q.
Executive Summary
We are a global medical technology company headquartered in Lewisville, Texas. By providing medical technologies that heal musculoskeletal pathologies, we deliver exceptional experiences and life-changing solutions to patients around the world. We offer a comprehensive portfolio of spinal hardware, bone growth therapies, specialized orthopedic solutions, biologics, and enabling technologies, including the 7D FLASH navigation system. To learn more, visit Orthofix.com and follow on LinkedIn. Information included on our website is not incorporated into, or otherwise creates a part of, this report.
Notable financial metrics in the second quarter of 2025 and recent achievements include the following:
•
Second quarter 2025 net sales of $203.1 million, including sales from our M6 artificial cervical and lumbar discs, and pro forma net sales of $200.7 million, excluding sales from our M6 discs, representing an increase of 2% on a reported basis and 4% on a pro forma constant currency basis compared to second quarter 2024
•
U.S. Spine Fixation net sales growth of 5% and procedure volume growth of 7% compared to second quarter 2024
•
Bone Growth Therapies ("BGT") net sales of $62.6 million, representing growth of 6%, with BGT Fracture net sales growth of 7% compared to second quarter 2024
•
Global Orthopedics net sales of $33.3 million, achieving constant currency growth of 5%, and U.S. Orthopedics net sales growth of 28% compared to second quarter 2024
•
Initiated global commercial launch of the TrueLok Elevate Transverse Bone Transport ("TBT") System – the first FDA-cleared device for TBT to correct non-unions and bony or soft tissue deformities or defects
•
Announced U.S. commercial launch of the Reef L Interbody System – completes Reef interbody product family with a full-spectrum solution for lateral lumbar spinal fusion procedures
•
Second quarter 2025 net loss of $(14.1) million on a reported basis; Non-GAAP pro forma adjusted EBITDA of $20.6 million, with pro forma adjusted EBITDA margin expanding approximately 190 basis points compared to reported non-GAAP adjusted EBITDA for the second quarter 2024
•
Six consecutive quarters of adjusted EBITDA margin expansion; positive free cash flow of $4.5 million for second quarter 2025
Results of Operations
The following table provides certain items in our condensed consolidated statements of operations as a percent of net sales:
Three Months Ended
June 30,
Six Months Ended
June 30,
(Unaudited)
2025
(%)
2024
(%)
2025
(%)
2024
(%)
Net sales
100.0
100.0
100.0
100.0
Cost of sales
31.3
32.2
34.2
32.3
Gross profit
68.7
67.8
65.8
67.7
Sales, general, and administrative
67.3
67.5
67.9
68.7
Research and development
7.8
9.1
9.0
9.7
Acquisition-related amortization, impairment, and remeasurement
1.5
3.7
5.3
3.3
Operating loss
(7.9
)
(12.5
)
(16.4
)
(14.0
)
Net loss
(6.9
)
(16.8
)
(16.9
)
(17.9
)
23
Net Sales by Product Category and Reporting Segment
Our operations are managed through two reporting segments: Global Spine and Global Orthopedics. The following table provides net sales by product category by reporting segment:
Three Months Ended June 30,
(Unaudited, U.S. Dollars, in millions)
2025
2024
Change
Constant
Currency
Change
Bone Growth Therapies
$
62.6
$
59.1
5.8
%
5.8
%
Spinal Implants, Biologics and Enabling Technologies*
104.8
103.1
1.6
%
1.6
%
Global Spine*
167.4
162.2
3.2
%
3.2
%
Global Orthopedics
33.3
30.6
8.9
%
5.3
%
Pro forma net sales*
200.7
192.8
4.1
%
3.5
%
Impact from discontinuation of M6 product lines
2.5
5.8
(57.5
%)
(57.8
%)
Reported net sales
$
203.1
$
198.6
2.3
%
1.7
%
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in millions)
2025
2024
Change
Constant
Currency
Change
Bone Growth Therapies
$
117.6
$
111.6
5.4
%
5.4
%
Spinal Implants, Biologics and Enabling Technologies*
209.1
205.4
1.8
%
1.8
%
Global Spine*
326.7
317.0
3.1
%
3.1
%
Global Orthopedics
63.1
57.9
9.0
%
8.2
%
Pro forma net sales*
389.8
374.9
4.0
%
3.9
%
Impact from discontinuation of M6 product lines
6.9
12.3
(44.0
%)
(43.9
%)
Reported net sales
$
396.7
$
387.2
2.5
%
2.4
%
* Results above for each of Spinal Implants, Biologics, and Enabling Technologies; Global Spine; and pro forma net sales exclude the impact of the Company's discontinuation of its M6 product lines. As pro forma net sales represent a Non-GAAP measure, see the reconciliation above of the Company's pro forma net sales to its reported figures under U.S. GAAP. The Company's reported figures under U.S. GAAP represent each of the pro forma line items discussed above plus the impact from discontinuation of the M6 product lines shown above
.
Global Spine
Global Spine offers the following product categories:
-
Bone Growth Therapies, which manufactures, distributes, sells, and provides support services for market-leading devices used adjunctively in high-risk spinal fusion procedures and treats both nonunion and acute fractures in the orthopedic space. Bone Growth Therapies uses distributors and a direct sales channel to sell its devices and provide associated support services to hospitals, healthcare providers, and patients in the U.S.
-
Spinal Implants, Biologics, and Enabling Technologies is comprised of a broad portfolio of spine fixation implant products used in surgical procedures of the spine, which includes one of the most comprehensive biologics portfolios in both the demineralized bone matrix and cellular allograft market segments and image-guided surgical solutions to facilitate degenerative, minimally invasive, and complex surgical procedures. Spinal Implants, Biologics, and Enabling Technologies products are sold through a network of distributors and sales representatives to hospitals and healthcare providers on a global basis for Spinal Implants and Enabling Technologies, and primarily within the U.S. for Biologics.
Three months ended June 30, 2025 compared to 2024
Net sales of $169.8 million, an increase of $1.8 million or 1.1%
•
Bone Growth Therapies net sales increased $3.4 million, or 5.8%, largely driven by (i) favorable changes in average sales prices, (ii) increase in gross order volumes from our continued investment in our direct sales channels for both the spine and fracture markets, and (iii) continued share growth of AccelStim
24
•
Spinal Implants, Biologics, and Enabling Technologies net sales, excluding sales from the M6 product lines, increased $1.7 million, or 1.6%, primarily due to increased sales growth from new and existing high-volume distribution partners, particularly within Spinal Implants, which saw growth in its cervical and thoracolumbar franchises; growth in these areas were partially offset by a decline in Biologics net sales
•
Net sales from the M6 product lines decreased $3.3 million, or 57.6%, as a result of the announcement and discontinuation of the product lines to focus resources and investment in more profitable growth opportunities
Six months ended June 30, 2025 compared to 2024
Net sales of $333.7 million, an increase of $4.3 million or 1.3%
•
Bone Growth Therapies net sales increased $6.0 million, or 5.4%, largely driven by (i) favorable changes in average sales prices, (ii) increase in gross order volumes from our continued investment in our direct sales channels for both the spine and fracture markets, and (iii) continued share growth of AccelStim
•
Spinal Implants, Biologics, and Enabling Technologies net sales, excluding sales from the M6 product lines, increased $3.7 million, or 1.8%, primarily due to increased sales growth from new and existing high-volume distribution partners, particularly within Spinal Implants, which saw growth in each of cervical, interbody, thoracolumbar, and spine fixation franchises; growth in these areas were partially offset by a decline in Biologics net sales
•
Net sales from the M6 product lines decreased $5.4 million, or 44.0%, as a result of the announcement and discontinuation of the product lines to focus resources and investment in more profitable growth opportunities
Global Orthopedics
Global Orthopedics offers products and solutions for the underserved limb reconstruction market that encompasses four pillars: deformity correction, limb lengthening, complex fracture management, and limb preservation. Global Orthopedics sells its products through a global network of distributors and sales representatives to hospitals, healthcare organizations, and healthcare providers.
Three months ended June 30, 2025 compared to 2024
Net sales of $33.3 million, an increase of $2.7 million or 8.9% on a reported basis and 5.3% on a constant currency basis
•
U.S. growth of $2.1 million, or 27.7%, largely due to investments made in recent product launches, commercial execution within our sales channel, and from growth within our TrueLok and Fitbone product lines
•
International sales decreased $0.5 million, or 2.2% on a constant currency basis, primarily driven by large orders made by non-governmental organizations in the prior year partially offset by growth within our TrueLok and Fitbone product lines in Europe
•
Increase of $1.1 million due to movement in foreign currency exchange rates, which had a favorable impact on net sales in the quarter
Six months ended June 30, 2025 compared to 2024
Net sales of $63.1 million, an increase of $5.2 million or 9.0% on a reported basis and 8.2% on a constant currency basis
•
U.S. growth of $3.0 million, or 18.7%, largely due to investments made in recent product launches, commercial execution within our sales channel, and from growth within our TrueLok, Fitbone, and OSCAR PRO product lines
•
International growth of $1.8 million, or 4.3% on a constant currency basis, primarily driven by recent product launches in Europe and timing of certain tender offers and stocking distributor orders
•
Increase of $0.4 million due to movement in foreign currency exchange rates, which had a favorable impact on net sales in the quarter
25
Gross Profit
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Net sales
$
203,121
$
198,620
2.3
%
$
396,767
$
387,228
2.5
%
Cost of sales
63,588
63,871
(0.4
%)
135,615
125,237
8.3
%
Gross profit
$
139,533
$
134,749
3.6
%
$
261,152
$
261,991
(0.3
%)
Gross margin
68.7
%
67.8
%
0.9
%
65.8
%
67.7
%
-1.8
%
Three months ended June 30, 2025 compared to 2024
Gross profit increased $4.8 million
•
Increase in gross profit of $3.0 million driven by a reduction of amortization of the inventory fair value step-up recognized in the merger with SeaSpine Holdings Corporation (the "SeaSpine Merger"), which were amortized over the expected sales cycles of the acquired inventory and concluded in December 2024
•
Increase in gross profit also driven by net sales growth across all principal product categories and from reduced headcount and overhead costs as a result of our decision to discontinue the M6 product lines
•
Partially offset by an increase in inventory reserve expenses of $2.8 million, primarily driven by our decision to discontinue the M6 product lines in order to focus resources and investments on more profitable growth opportunities
Six months ended June 30, 2025 compared to 2024
Gross profit decreased $0.8 million
•
Decrease in gross profit of $11.6 million resulting from an increase in inventory reserve expenses, primarily driven by our decision to discontinue the M6 product lines in order to focus resources and investments on more profitable growth opportunities
•
Partially offset by increase in gross profit of $6.1 million driven by a reduction of amortization of the inventory fair value step-up recognized in the SeaSpine Merger, which were amortized over the expected sales cycles of the acquired inventory and concluded in December 2024
•
Further offset by an increase in gross profit driven by net sales growth across all principal product categories
Sales, General, and Administrative Expense
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Sales, general, and administrative
$
136,493
$
134,218
1.7
%
$
269,474
$
265,909
1.3
%
As a percentage of net sales
67.2
%
67.6
%
(0.4
%)
67.9
%
68.7
%
(0.8
%)
Three months ended June 30, 2025 compared to 2024
Sales, general, and administrative expense increased $2.3 million
•
Increase of approximately $4.0 million in compensation related costs, including variable compensation, due to the increase in net sales and from increased headcount
•
Increase of $3.9 million associated with certain legal matters, including our ongoing arbitration claims with former executives and the related securities class action complaints
•
Partially offset by a decrease of $5.3 million in succession charges as a result of changes made in our executive leadership positions in the prior year
Six months ended June 30, 2025 compared to 2024
Sales, general, and administrative expense increased $3.6 million
•
Increase of $7.4 million related to impairments on certain assets and losses incurred as a result of our decision to discontinue the M6 product lines
26
•
Increase of $4.6 million associated with certain legal matters, including our ongoing arbitration claims with former executives and the related securities class action complaints
•
Partially offset by a decrease of $6.1 million in succession charges as a result of changes made in our executive leadership positions in the prior year
•
Partially offset by a decrease of $2.3 million in integration-related costs, mostly stemming from severance expenses and professional fees incurred in the prior year
Research and Development Expense
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Research and development
$
15,934
$
18,049
(11.7
%)
$
35,700
$
37,541
(4.9
%)
As a percentage of net sales
7.8
%
9.1
%
(1.3
%)
9.0
%
9.7
%
(0.7
%)
Three months ended June 30, 2025 compared to 2024
Research and development expense decreased $2.1 million
•
Primarily due to synergies achieved of around $2.5 million in comparison to the second quarter of 2024 as a result of our recent restructuring activities, mostly related to headcount, professional fees, and reduced spend for clinical studies as a result of our decision to discontinue the M6 product lines
•
Partially offset by an increase in legal settlement expenses of $0.5 million
Six months ended June 30, 2025 compared to 2024
Research and development expense decreased $1.8 million
•
Primarily due to synergies achieved of around $6.0 million in comparison to 2024 as a result of our recent restructuring activities, mostly related to headcount, professional fees, and reduced spend for clinical studies as a result of our decision to discontinue the M6 product lines
•
Further driven by a reduction of $0.7 million in costs to comply with the European Union Medical Device Regulations
•
Partially offset by $3.7 million related to the impairments associated with our discontinuation of the M6 product lines and other organizational restructuring activities
•
Partially offset by an increase in legal settlement expenses of $0.5 million
Acquisition-related Amortization, Impairment, and Remeasurement
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Acquisition-related amortization, impairment, and remeasurement
$
3,109
$
7,388
(57.9
%)
$
20,854
$
12,784
63.1
%
As a percentage of net sales
1.5
%
3.7
%
(2.2
%)
5.3
%
3.2
%
2.1
%
Acquisition-related amortization, impairment, and remeasurement consists of (i) amortization and impairment related to intangible assets acquired through business combinations or asset acquisitions and (ii) remeasurement of related contingent consideration arrangements, which are recognized immediately upon acquisition.
Three months ended June 30, 2025 compared to 2024
Acquisition-related amortization, impairment, and remeasurement decreased $4.3 million
•
Decrease of $3.8 million associated with the remeasurement of a contingent consideration obligation with Lattus Spine LLC assumed in the SeaSpine Merger
•
Decrease of $0.4 million in amortization expense of acquired intangibles, primarily as a result of our decision in the first quarter of 2025 to discontinue the M6 product lines and other product portfolio decisions
27
Six months ended June 30, 2025 compared to 2024
Acquisition-related amortization, impairment, and remeasurement increased $8.1 million
•
Increase of $13.7 million in amortization and impairment expense of acquired intangibles, primarily associated with the impairment of certain acquired intangible assets as a result of the discontinuation of the M6 product lines and other product portfolio decisions
•
Partially offset by a decrease of $5.6 million associated with the remeasurement of a contingent consideration obligation with Lattus Spine LLC assumed in the SeaSpine Merger
Non-operating Income and Expense
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Interest expense, net
$
(3,950
)
$
(4,943
)
(20.1
%)
$
(8,456
)
$
(9,501
)
(11.0
%)
Other income/(expense), net
5,730
(2,510
)
(328.3
%)
6,976
(3,784
)
(284.4
%)
Three months ended June 30, 2025 compared to 2024
Interest expense, net decreased $1.0 million
•
Favorable change of $0.8 million associated with interest earned associated with certain Employee Retention Credit refunds received during the second quarter of 2025
•
Favorable change of $0.3 million attributable to a decrease in interest expense resulting from the amortization of debt issuance costs
Other income (expense), net increased
$8.2 million
•
Favorable change of $3.6 million associated with foreign currency exchange rates, as we recorded a non-cash remeasurement gain of $2.7 million in the second quarter of 2025 compared to a loss of $0.9 million in the second quarter of 2024
•
Increase of $2.8 million associated with the receipt of Employee Retention Credit refunds received during the second quarter of 2025
•
Increase of $1.4 million associated with the impairment of certain investments measured at fair value in the prior year
Six months ended June 30, 2025 compared to 2024
Interest expense, net decreased $1.0 million
•
Favorable change of $0.8 million associated with interest earned associated with certain Employee Retention Credit refunds received during the second quarter of 2025
•
Favorable change of $0.7 million attributable to a decrease in interest expense resulting from the amortization of debt issuance costs
•
Partially offset by a decrease of $0.3 million of interest income as a result of the conversion of our former convertible loan with Neo Medical into preferred equity securities in the second quarter of 2024
Other income (expense), net increased
$10.8 million
•
Favorable change of $6.2 million associated with foreign currency exchange rates, as we recorded a non-cash remeasurement gain of $3.8 million in 2025 compared to a loss of $2.4 million in 2024
•
Increase of $2.8 million associated with the receipt of Employee Retention Credit refunds received during the second quarter of 2025
•
Increase of $1.4 million associated with the impairment of certain investments measured at fair value in the prior year
28
Income Taxes
Three Months Ended June 30,
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
% Change
2025
2024
% Change
Income tax (benefit) expense
$
(142
)
$
1,084
(113.1
%)
$
819
$
1,935
(57.7
%)
Effective tax rate
1.0
%
(3.3
%)
4.3
%
(1.2
%)
(2.9
%)
1.7
%
Three months ended June 30, 2025 compared to 2024
•
The decrease in tax expense compared to the prior year period is primarily due to decreased tax on foreign operations and tax benefit related to certain long-lived intangible assets
•
The primary factor affecting our tax expense for the second quarter of 2025 compared to the prior year period was tax amortization on certain acquired intangibles and financial statement losses not benefitted
Six months ended June 30, 2025 compared to 2024
•
The decrease in tax expense compared to the prior year period is primarily due to decreased tax on foreign operations and tax benefit related to certain long-lived intangible assets
•
The primary factor affecting our tax expense for the second quarter of 2025 compared to the prior year period was tax amortization on certain acquired intangibles and financial statement losses not benefitted
Liquidity and Capital Resources
Cash, cash equivalents, and restricted cash at June 30, 2025, totaled $68.7 million compared to $85.7 million at December 31, 2024. The following table presents the net change in cash, cash equivalents, and restricted cash for the six months ended June 30, 2025, and 2024, respectively:
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Change
Net cash used in operating activities
$
(6,752
)
$
(9,611
)
$
2,859
Net cash used in investing activities
(13,833
)
(20,583
)
6,750
Net cash provided by financing activities
1,989
21,678
(19,689
)
Effect of exchange rate changes on cash
1,547
(375
)
1,922
Net change in cash and cash equivalents
$
(17,049
)
$
(8,891
)
$
(8,158
)
The following table presents free cash flow, a non-GAAP financial measure, which is calculated by subtracting capital expenditures from net cash from operating activities:
Six Months Ended June 30,
(Unaudited, U.S. Dollars, in thousands)
2025
2024
Change
Net cash used in operating activities
$
(6,752
)
$
(9,611
)
$
2,859
Capital expenditures
(13,845
)
(20,533
)
6,688
Free cash flow
$
(20,597
)
$
(30,144
)
$
9,547
Operating Activities
Cash flows from operating activities increased $2.9 million
•
Favorable change in net loss of $2.3 million
•
Favorable change of $6.9 million associated with non-cash gains and losses, such as depreciation and amortization, inventory reserve expenses, the amortization of the inventory fair value step-up recognized in the SeaSpine Merger, remeasurement of contingent consideration obligations, and share-based compensation expense
•
Unfavorable change of $6.3 million relating to changes in working capital accounts, primarily attributable to changes in other current assets and accounts receivable
29
Two of our primary working capital accounts are accounts receivable and inventory. Days sales in receivables were 58 days at June 30, 2025, compared to 57 days at June 30, 2024 (calculated using second quarter net sales and ending accounts receivable). Inventory turns improved to 1.5 times as of June 30, 2025 compared to 1.2 times as of June 30, 2024 (calculated using trailing twelve-month cost of goods sold and ending net inventories).
Investing Activities
Cash flows used in investing activities decreased $6.8 million
•
Decrease in spend of $6.7 million in capital expenditures
Financing Activities
Cash flows from financing activities decreased $19.7 million
•
Decrease of $25.0 million associated with net borrowing activities related to our credit facilities
•
Partially offset by an increase of $3.5 million in net proceeds from the issuance of common shares
•
Further offset by a favorable change of $1.9 million in debt issuance costs associated with our credit facilities
Credit Facilities
On November 7, 2024, we entered into a $275.0 million secured credit agreement (the "Credit Agreement") with Oxford Finance LLC, as administrative agent and as collateral agent ("Oxford") and certain lenders party thereto, including Oxford, K2 HealthVentures LLC, and HSBC Ventures USA Inc. Certain of our foreign subsidiaries joined the Credit Agreement as guarantors shortly after the signing date. The Credit Agreement provides for a $160.0 million senior secured term loan (the "Initial Term Loan") and a $65.0 million senior secured delayed draw term loan facility (the "Term B Loan"). Draws under the Term B Loan are at our option from January 1, 2025 through June 30, 2026, subject to, among other conditions, our continued compliance with a pro-forma total debt-to-EBITDA leverage ratio of less than 4.0x. EBITDA is a non-GAAP financial measure which represents earnings before interest income (expense), income taxes, depreciation, amortization, and other negotiated addbacks and adjustments. In addition, at Oxford's discretion, an additional $50.0 million of draw capacity is available through January 1, 2029 (the "Term C Loan" and, together with the Term B Loan, the "Delayed Draw Term Loans" and collectively with the Initial Term Loan, the "Credit Facilities"). The Initial Term Loan and Delayed Draw Term Loans, to the extent ultimately drawn, will each mature in November 2029, following an interest-only payment period ending December 2028, and monthly amortization of principal and accrued interest between January 2029 and November 2029.
The Credit Agreement contains financial covenants requiring us to maintain a minimum level of liquidity at all times and to maintain a maximum total debt-to-EBITDA leverage ratio (measured on a quarterly basis) during the term of the facility. As of June 30, 2025, we were in compliance with all required financial covenants.
As of June 30, 2025, we had $160.0 million of outstanding borrowings under the Credit Agreement related to the Initial Term Loan. We have not made any borrowings under the Delayed Draw Term Loans as of June 30, 2025.
As of June 30, 2025, we had no borrowings on our available lines of credit in Italy, which provide up to an aggregate amount of €5.5 million ($6.5 million).
Other
For information regarding contingencies, see Note 7 to the Notes to the Unaudited Condensed Consolidated Financial Statements contained herein.
Under the terms of a contingent consideration obligation in a purchase agreement assumed in the SeaSpine Merger, we may be required to make installment payments at certain dates based on future net sales of certain products (the "Lateral Products"). The estimated fair value of the contingent consideration arrangement as of June 30, 2025, was $14.0 million; however, the actual amount ultimately paid could be higher or lower than the estimated fair value of the contingent consideration. As of June 30, 2025, we classified the remaining contingent consideration liability of $10.5 million and $3.5 million within other current liabilities and
30
other long-term liabilities, respectively. For additional discussion of this matter, see Note 6 of the Notes to the Unaudited Condensed Consolidated Financial Statements.
Off-balance Sheet Arrangements
As of June 30, 2025, we did not have any off-balance sheet arrangements that have or are reasonably likely to have a current or future effect on our financial condition, changes in financial condition, revenues or expenses, results of operations, cash flows, liquidity, capital expenditures or capital resources that are material to investors.
Contractual Obligations
There have been no material changes in any of our material contractual obligations as disclosed in our Form 10-K for the year ended December 31, 2024.
Critical Accounting Estimates
Our discussion of operating results is based upon the condensed consolidated financial statements and accompanying notes. The preparation of these statements requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amount of revenues and expenses during the reporting period. Our critical accounting estimates are described in Item 7 of our Annual Report on Form 10-K for the year ended December 31, 2024. There have been no significant changes to our critical accounting estimates during the quarter covered by this report.
Recently Issued Accounting Pronouncements
See Note 2 of the Notes to the Unaudited Condensed Consolidated Financial Statements for detailed information regarding the status of recently issued or adopted accounting pronouncements.
Non-GAAP Financial Measures
We believe that providing non-GAAP financial measures that exclude certain items provides investors with greater transparency to the information used by senior management in its financial and operational decision-making. We believe it is important to provide investors with the same non-GAAP financial measures used to supplement information regarding the performance and underlying trends of our business operations to facilitate comparisons to historical operating results and internally evaluate the effectiveness of our operating strategies. Disclosure of these non-GAAP financial measures also facilitates comparisons of our underlying operating performance with other companies in the industry that also supplement their U.S. GAAP results with non-GAAP financial measures.
The non-GAAP financial measures used in this filing may have limitations as analytical tools and should not be considered in isolation or as a replacement for U.S. GAAP financial measures. Some limitations associated with the use of these non-GAAP financial measures are that they exclude items that reflect an economic cost that can have a material effect on cash flows.
Constant Currency
Constant currency is calculated by using foreign currency rates from the comparable, prior year period to present net sales at comparable rates. Constant currency can be presented for numerous U.S. GAAP measures but is most commonly used by management to analyze net sales without the impact of changes in foreign currency rates.
Free Cash Flow
Free cash flow is calculated by subtracting capital expenditures from net cash from operating activities. Management uses free cash flow as an important indicator of how much cash is generated or used by our normal business operations, including capital expenditures. Management uses free cash flow as a measure of progress on its capital efficiency and cash flow initiatives.
I
tem 3. Quantitative and Qualitative Disclosures About Market Risk
There have been no material changes to our market risks as disclosed in our Form 10-K for the year ended December 31, 2024.
31
I
tem 4. Controls and Procedures
Evaluation of Disclosure Controls and Procedures
We maintain disclosure controls and procedures (as defined in Rule 13a-15(e) of the Exchange Act) designed to provide reasonable assurance that the information required to be disclosed in reports filed or submitted under the Exchange Act are recorded, processed, summarized, and reported within the time periods specified in the SEC's rules and forms. These include controls and procedures designed to ensure that this information is accumulated and communicated to management, including our Chief Executive Officer and our Chief Financial Officer, as appropriate to allow timely decisions regarding required disclosure. Management, with the participation of the Chief Executive Officer and the Chief Financial Officer, evaluated the effectiveness of our disclosure controls and procedures as of June 30, 2025. Based on this evaluation, our Chief Executive Officer and our Chief Financial Officer have concluded that our disclosure controls and procedures were effective as of June 30, 2025.
Changes in Internal Control over Financial Reporting
There was no change in our internal control over financial reporting that occurred during the quarterly period covered by this report that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
32
PART II. OTHER
INFORMATION
Item 1. Legal
Proceedings
For information regarding legal proceedings, see Note 7 to the Notes to the Unaudited Condensed Consolidated Financial Statements contained herein, which is incorporated by reference into this Part II, Item 1.
Item 1A. Ris
k Factors
There have been no material changes from the risk factors disclosed in "Part I, Item 1A. Risk Factors" in our Form 10-K for the year ended December 31, 2024.
Item 2. Unregistered Sales of Equit
y Securities and Use of Proceeds
We have not made any repurchases of our common stock during the second quarter of 2025.
Item 3. Defaults Upo
n Senior Securities
Not applicable.
Item 4. Mine Saf
ety Disclosures
Not applicable.
Item 5. Other
Information
During the last fiscal quarter, none of our
directors or officers
(as defined in Rule 16a-1(f) of the Exchange Act)
adopted
,
modified
or
terminated
any contract, instruction, or written plan for the purchase or sale of our securities that was intended to satisfy the affirmative defense conditions of Rule 10b5-1(c) of the Exchange Act or any "non-Rule 10b5-1 trading arrangement."
Inline XBRL Instance Document (the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document).
Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101).
* Filed herewith.
† Certain private and confidential portions of this exhibit that are not material were omitted by means of redacting a portion of the text and replacing it with a bracketed asterisk.
# Furnished herewith.
33
SIGNAT
URES
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
Customers and Suppliers of Orthofix Medical Inc.
Beta
No Customers Found
No Suppliers Found
Bonds of Orthofix Medical Inc.
Price Graph
Price
Yield
Insider Ownership of Orthofix Medical Inc.
company Beta
Owner
Position
Direct Shares
Indirect Shares
AI Insights
Summary Financials of Orthofix Medical Inc.
Beta
(We are using algorithms to extract and display detailed data. This is a hard problem and we are working continuously to classify data in an accurate and useful manner.)
