Xtant Medical Reports Second Quarter 2025 Financial Results
Total Revenue of
Delivers Positive Net Income, Adjusted EBITDA and Operating Cash Flow
Raises FY25 Revenue Guidance to
Second Quarter 2025 Financial Highlights
- Revenue of
$35.4 million , up 18%, compared to the prior year quarter - Gross margin of 68.6% compared to 62.1% for the prior year quarter
- Net income of
$3.6 million compared to a net loss of$3.9 million in the prior year quarter - Adjusted EBITDA of
$6.9 million compared to Adjusted EBITDA loss of$0.6 million in the prior year quarter - Cash generated from operations of
$1.2 million compared to cash used in operations of$5.1 million in the prior year quarter - Raised FY25 revenue guidance to
$131-$135 million , representing growth of 11%-15%, excluding the impact of the pending sale of certain assets to Companion Spine
Recent Business Highlights
- Announced definitive agreements to sell its non-core Coflex® and CoFix® spinal implants and all OUS businesses to Companion Spine for total proceeds of approximately
$19.2 million - Launched OsteoFactor Pro™, a naturally occurring cocktail of allogeneic growth factors engineered and designed to improve bone healing and support surgical success across orthopedic and spine procedures
- Launched Trivium™, a premium, next-generation demineralized bone matrix (DBM) allograft designed to elevate the standard of care in bone grafting procedures
Second Quarter 2025 Financial Results
Revenue grew 18% to
Gross margin for the second quarter of 2025 was 68.6%, compared to 62.1% for the same period in 2024. The increase is primarily attributable to the impact of royalty revenue in the current year period, as well as lower product costs and greater scale.
Operating expenses for the second quarter of 2025 totaled
Net income totaled
Non-GAAP adjusted EBITDA for the second quarter of 2025 totaled
The Company defines adjusted EBITDA as net income/loss from operations before depreciation, amortization and interest expense and provision for income tax/benefit, and as further adjusted to add back in or exclude, as applicable, separation-related expenses, non-cash compensation, disposition/acquisition-related expense, acquisition-related fair value adjustments and unrealized foreign currency translation gain or loss. A calculation and reconciliation of adjusted EBITDA to net loss can be found in the attached financial tables.
As of
2025 Financial Guidance
Xtant is raising its full-year 2025 revenue guidance to a range of
Conference Call
To access the webcast, visit Webcast Link: https://www.webcaster4.com/Webcast/Page/3039/52698
To access the conference call, dial 877-545-0523 (US) or 973-528-0016 (International) and reference Participant Access Code 482755.
A replay of the call will be available on the Investor section of the Company's website at www.xtantmedical.com.
About
The symbols ™ and ® denote trademarks and registered trademarks of
Non-GAAP Financial Measures
To supplement the Company's consolidated financial statements prepared in accordance with
Cautionary Statement Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements that are predictive in nature, that depend upon or refer to future events or conditions, or that include words such as "intends," ''expects,'' ''anticipates,'' ''plans,'' ''believes,'' ''estimates,'' "continue," "future," ''will,'' "potential," "going forward," "guidance," similar expressions or the negative thereof, and the use of future dates. Forward-looking statements in this release include the Company's full year 2025 revenue guidance and the anticipated closing of the sale of the Company's Coflex® and CoFix® spinal implants and all OUS businesses to Companion Spine and proceeds therefrom. The Company cautions that its forward-looking statements by their nature involve risks and uncertainties, and actual results may differ materially depending on a variety of important factors, including, among others: the possibility that the sale of the Company's Coflex and CoFix products and international business are not completed or, if completed, that the anticipated benefits of the transactions are not realized when expected or at all; the possibility that the transactions may be more expensive to complete than anticipated; diversion of management's attention from ongoing business operations and opportunities; the occurrence of any event, change or other circumstances that could give rise to the right of the parties to terminate either or both transactions; exposure to potential litigation and adverse tax consequences; the Company's future operating results and financial performance; its ability to increase or maintain revenue; the Company's ability to become operationally self-sustaining and less reliant on third-party manufacturers and suppliers; risks associated with its acquisitions and the integration of those businesses; anticipated shortages of stem cells which will adversely affect future revenues; the ability to implement successfully its future growth initiatives and risks associated therewith; possible future impairment charges to long-lived assets and goodwill and write-downs of excess inventory; the ability to remain competitive; the ability to innovate, develop and introduce new products and the success of those products; the ability to engage and retain new and existing independent distributors and agents and qualified personnel and the Company's dependence on key independent agents for a significant portion of its revenue; the effect of labor and hospital staffing shortages on the Company's business, operating results and financial condition, especially when they affect key markets; the effect of inflation, increased interest rates and other recessionary factors and supply chain disruptions; the effect of product sales mix changes on the Company's financial results; government and third-party coverage and reimbursement for Company products; the ability to obtain and maintain regulatory approvals and comply with government regulations; the effect of product liability claims and other litigation to which the Company may be subject; the effect of product recalls and defects; the ability to license certain of the Company's intellectual property on commercially reasonable terms and to maintain any such licenses; the ability to obtain and protect Company intellectual property and proprietary rights and operate without infringing the rights of others; risks associated with the Company's clinical trials; international risks; the ability to service Company debt, comply with its debt covenants and access additional indebtedness; the ability to maintain sufficient liquidity to fund its operations and obtain financing on favorable terms or at all; and other factors. Additional risk factors are contained in the Company's Annual Report on Form 10-K for the year ended
-- Tables Follow –
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As of |
As of December |
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ASSETS |
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Current Assets: |
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|
|
|
Cash and cash equivalents |
|
$ 6,923 |
|
$ 6,199 |
Restricted cash |
|
114 |
|
22 |
Trade accounts receivable, net of allowance for credit losses and doubtful accounts of |
26,951 |
|
20,660 |
|
Inventories |
|
40,135 |
|
38,634 |
Prepaid and other current assets |
|
1,466 |
|
1,601 |
Total current assets |
|
75,589 |
|
67,116 |
|
|
|
|
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Property and equipment, net |
|
10,447 |
|
10,131 |
Right-of-use asset, net |
|
2,634 |
|
829 |
|
|
7,302 |
|
7,302 |
Intangible assets, net |
|
7,492 |
|
8,356 |
Other assets |
|
15 |
|
103 |
Total Assets |
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$ 103,479 |
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$ 93,837 |
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LIABILITIES & STOCKHOLDERS' EQUITY |
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Current Liabilities: |
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Accounts payable |
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$ 7,223 |
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$ 7,918 |
Accrued liabilities |
|
10,626 |
|
7,771 |
Current portion of lease liability |
|
693 |
|
703 |
Current portion of finance lease obligations |
|
52 |
|
69 |
Line of credit |
|
12,006 |
|
12,120 |
Total current liabilities |
|
30,600 |
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28,581 |
Long-term Liabilities: |
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|
|
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Lease liability, less current portion |
|
2,015 |
|
166 |
Financing lease obligations, less current portion |
|
30 |
|
47 |
Long-term debt, plus premium and less issuance costs |
|
22,278 |
|
22,038 |
Other liabilities |
|
54 |
|
42 |
Total Liabilities |
|
54,977 |
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50,874 |
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Stockholders' Equity |
|
|
|
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Preferred stock, |
- |
|
- |
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Common stock, |
- |
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- |
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Additional paid-in capital |
|
304,201 |
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302,738 |
Accumulated other comprehensive income (loss) |
|
152 |
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(316) |
Accumulated deficit |
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(255,851) |
|
(259,459) |
Total Stockholders' Equity |
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48,502 |
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42,963 |
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Total Liabilities & Stockholders' Equity |
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$ 103,479 |
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$ 93,837 |
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Three Months Ended |
Six Months Ended |
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2025 |
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2024 |
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2025 |
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2024 |
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Revenue |
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Product revenue |
|
|
|
|
|
|
|
|
|
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License revenue |
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4,975 |
|
- |
|
8,595 |
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- |
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Total Revenue |
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35,411 |
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29,943 |
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68,315 |
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57,816 |
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Cost of Sales |
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11,127 |
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11,361 |
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23,788 |
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21,932 |
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Gross Profit |
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24,284 |
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18,582 |
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44,527 |
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35,884 |
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Gross Profit % |
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68.6 % |
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62.1 % |
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65.2 % |
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62.1 % |
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Operating Expenses |
|
|
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General and administrative |
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7,478 |
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7,713 |
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15,011 |
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15,498 |
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Sales and marketing |
|
11,616 |
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13,179 |
|
22,820 |
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25,639 |
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Research and development |
|
566 |
|
636 |
|
1,009 |
|
1,163 |
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Total Operating Expenses |
|
19,660 |
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21,528 |
|
38,840 |
|
42,300 |
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|
|
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|
|
|
|
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|
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Income (Loss) from Operations |
|
4,624 |
|
(2,946) |
|
5,687 |
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(6,416) |
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Other Expense |
|
|
|
|
|
|
|
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Interest expense |
|
(1,004) |
|
(992) |
|
(2,049) |
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(1,827) |
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|
Unrealized foreign currency translation gain |
|
178 |
|
118 |
|
202 |
|
79 |
|
|
Other income (expense) |
|
7 |
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(5) |
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(2) |
|
7 |
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Total Other Expense |
|
(819) |
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(879) |
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(1,849) |
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(1,741) |
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Net Income (Loss) from Operations Before Provision for Income Taxes |
3,805 |
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(3,825) |
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3,838 |
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(8,157) |
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Provision for Income Taxes |
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Current and Deferred |
|
(255) |
|
(36) |
|
(230) |
|
(104) |
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Net Income (Loss) |
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Net Income (Loss) Per Share: |
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Basic |
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$ 0.03 |
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|
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$ 0.03 |
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Dilutive |
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$ 0.02 |
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|
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$ 0.02 |
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Shares used in the computation: |
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Basic |
|
139,310,589 |
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130,269,710 |
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139,190,378 |
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130,291,796 |
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Dilutive |
|
148,574,242 |
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130,269,710 |
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148,339,423 |
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130,291,796 |
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Six Months Ended |
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2025 |
|
2024 |
Operating activities: |
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Net income (loss) |
|
$ 3,608 |
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|
Adjustments to reconcile net income (loss) to net cash provided by (used in) operating activities: |
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|
|
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Depreciation and amortization |
|
2,243 |
|
2,003 |
Gain on sale of fixed assets |
|
(49) |
|
(142) |
Non-cash interest |
|
289 |
|
218 |
Stock-based compensation |
|
1,524 |
|
2,138 |
Provision for reserve on accounts receivable |
|
395 |
|
178 |
Provision for excess and obsolete inventory |
|
490 |
|
388 |
Other |
|
46 |
|
1 |
Changes in operating assets and liabilities: |
|
|
|
|
Accounts receivable |
|
(6,873) |
|
(688) |
Inventories |
|
(1,349) |
|
(4,130) |
Prepaid and other assets |
|
347 |
|
(469) |
Accounts payable |
|
(880) |
|
(15) |
Accrued liabilities |
|
2,763 |
|
(2,064) |
Net cash provided by (used in) operating activities |
|
2,554 |
|
(10,843) |
Investing activities: |
|
|
|
|
Purchases of property and equipment |
|
(1,557) |
|
(1,337) |
Proceeds from sale of fixed assets |
|
97 |
|
183 |
Net cash used in investing activities |
|
(1,460) |
|
(1,154) |
Financing activities: |
|
|
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Payments on financing leases |
|
(34) |
|
(32) |
Borrowings on line of credit |
|
51,812 |
|
59,565 |
Repayments on line of credit |
|
(51,925) |
|
(52,288) |
Proceeds from issuance of long term debt |
|
- |
|
5,000 |
Debt issuance costs |
|
(49) |
|
(615) |
Payment of taxes from withholding of common stock on settlement of restricted stock units |
|
(61) |
|
(17) |
Net cash (used in) provided by financing activities |
|
(257) |
|
11,613 |
|
|
|
|
|
Effect of exchange rate changes on cash and cash equivalents and |
|
(21) |
|
(61) |
Net change in cash and cash equivalents and restricted cash |
|
816 |
|
(445) |
Cash and cash equivalents and restricted cash at beginning of year |
|
6,221 |
|
5,923 |
Cash and cash equivalents and restricted cash at end of year |
|
|
|
$ 5,478 |
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|
|
|
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Reconciliation of cash and cash equivalents and restricted cash |
|
|
|
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Cash and cash equivalents |
|
6,923 |
|
5,379 |
Restricted cash |
|
114 |
|
99 |
Total cash and restricted cash reported in the consolidated balance |
|
$ 7,037 |
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$ 5,478 |
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Three Months Ended |
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Six Months Ended |
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2025 |
2024 |
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2025 |
2024 |
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Net Income (Loss) |
|
$ 3,550 |
$ (3,861) |
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$ 3,608 |
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Depreciation and amortization |
|
1,169 |
998 |
|
2,243 |
2,003 |
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Interest expense |
|
1,004 |
992 |
|
2,049 |
1,827 |
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Tax (benefit) expense |
|
255 |
36 |
|
230 |
104 |
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Non-GAAP EBITDA |
|
5,978 |
(1,835) |
|
8,130 |
(4,327) |
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Non-GAAP EBITDA/Total revenue |
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16.9 % |
-6.1 % |
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11.9 % |
-7.5 % |
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NON-GAAP ADJUSTED EBITDA CALCULATION |
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|
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Separation related expenses |
|
(17) |
- |
|
23 |
- |
||
Non-cash compensation |
|
766 |
1,228 |
|
1,524 |
2,138 |
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Divestiture/acquisition-related expense |
|
295 |
- |
|
295 |
338 |
||
Acquisition-related fair value adjustments (1) |
|
60 |
129 |
|
171 |
384 |
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Unrealized foreign currency translation (gain) loss |
|
(178) |
(118) |
|
(202) |
(79) |
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Non-GAAP Adjusted EBITDA |
|
$ 6,904 |
$ (596) |
|
$ 9,941 |
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|
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Non-GAAP Adjusted EBITDA/Total revenue |
|
22.7 % |
-2.0 % |
|
16.6 % |
-2.7 % |
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(1) Beginning in the fourth quarter of 2024, phasing of the bargain purchase gain on sell through of inventory acquired as part of the purchase of Surgalign Holdings' hardware and biologics business is no longer included in acquisition-related fair value adjustments in the non-GAAP adjusted EBITDA calculation and prior period calculations as presented herein have been recast to conform to the current presentation and calculation. The related effect on adjusted EBITDA was a reduction of |
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