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Vericel raises 2026 revenue outlook to $344M–$346M

Vericel raised its full-year revenue and adjusted EBITDA margin outlook; third-quarter operating cash flow was below the year-earlier level.

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Form Type
8-K

Rhea-AI Filing Summary

Vericel Corporation (VCEL) reported third-quarter 2026 revenue of $85.4 million, up 26% from $67.5 million a year earlier. MACI revenue was $67.4 million, up 21%, and Burn Care revenue was $18.0 million, up 52%. Net income rose 179% to $14.2 million, or $0.27 per diluted share; adjusted EBITDA increased 48% to $25.2 million, or 30% of revenue. Gross margin was 73%, matching the prior-year quarter.

Operating cash flow was $17.7 million versus $22.1 million a year earlier, while free cash flow was $15.7 million versus $19.5 million. Vericel reported $235.6 million in cash and investments and no debt. It repurchased 220,744 shares for $8.8 million during the quarter; $191.2 million of repurchase authorization remained as of September 30, 2026.

Vericel raised 2026 revenue guidance to $344 million to $346 million from $330 million to $340 million, including MACI guidance of $290 million to $292 million and Burn Care guidance of $54 million. Adjusted EBITDA margin guidance rose to 28% from 27%, while gross margin guidance was reaffirmed at approximately 75%. The company said it remains on track for a potential MACI launch in the U.K. in 2027.

4 points · 1 major

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0 major · 1 point

Hollow bars mark forward-looking points. How the balance works

Positive

  • Major point. Forward-looking: it has not happened yet and may not happen.2026 revenue guidance rose to $344 million to $346 million.
  • Moderate pointRevenue grew 26% to $85.4 million in Q3 2026.
  • Moderate pointNet income rose 179% to $14.2 million in Q3 2026.
  • Moderate pointAdjusted EBITDA rose 48% to $25.2 million in Q3 2026.

Negative

  • Moderate pointOperating cash flow was $17.7 million, versus $22.1 million in Q3 2025.

Filing Explained

Through September 30, Vericel reported year-to-date net income of $10,065 thousand, versus a loss of $6,725 thousand a year earlier, and free cash flow of $45,066 thousand, versus $11,921 thousand.

Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Third-quarter revenue $85.4 million Q3 2026; 26% growth from $67.5 million in Q3 2025
Net income $14.2 million Q3 2026; 179% increase from $5.1 million in Q3 2025
Adjusted EBITDA $25.2 million Q3 2026; 48% increase from $17.0 million in Q3 2025
Operating cash flow $17.7 million Q3 2026, compared with $22.1 million in Q3 2025
Full-year revenue guidance $344 million to $346 million 2026 guidance, raised from $330 million to $340 million
Adjusted EBITDA margin guidance 28% 2026 guidance, raised from 27%
Shares repurchased 220,744 shares During Q3 2026, for $8.8 million; $191.2 million of authorization remained as of September 30, 2026
Cash and investments $235.6 million As of September 30, 2026; the company reported no debt
Adjusted EBITDA financial
"Non-GAAP adjusted EBITDA increased 48% to $25.2 million"
Adjusted EBITDA is a way companies measure how much money they make from their core operations, like running a business, by removing certain costs or income that aren’t part of regular business activities. It helps investors see how well a company is doing without distractions from unusual expenses or gains, making it easier to compare companies or track performance over time.
Free cash flow financial
"Free cash flow of $15.7 million"
Free cash flow is the amount of money a company has left over after paying all its expenses and investing in its business, like buying equipment or updating facilities. It shows how much cash is available to reward shareholders, pay down debt, or save for future growth. This helps investors understand if a company is financially healthy and able to grow.
autologous cultured chondrocytes medical
"MACI (autologous cultured chondrocytes on porcine collagen membrane)"
Autologous cultured chondrocytes are a patient’s own cartilage cells that are collected, grown in a lab to increase their number, and then re-implanted to repair damaged cartilage. For investors, these therapies matter because they represent a personalized medical product with potential for premium pricing, complex manufacturing and regulatory hurdles, and significant impact on surgical demand, reimbursement and long-term treatment costs—factors that affect commercial value and risk.
cultured epidermal autografts medical
"Epicel (cultured epidermal autografts)"
eschar removal medical
"indicated for eschar removal in adults and pediatric patients"
Revenue $85.4 million 26% growth from $67.5 million in Q3 2025
Net income $14.2 million 179% increase from $5.1 million in Q3 2025
Adjusted EBITDA $25.2 million 48% increase from $17.0 million in Q3 2025
Operating cash flow $17.7 million Compared with $22.1 million in Q3 2025
Guidance

Raised 2026 revenue guidance to $344 million to $346 million and adjusted EBITDA margin guidance to 28%.

FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

How did VCEL perform in Q3 2026?

Vericel reported $85.4 million in third-quarter revenue, up 26% from $67.5 million in the prior-year quarter. Net income was $14.2 million, and non-GAAP adjusted EBITDA was $25.2 million, equal to 30% of revenue.

What is VCEL's updated 2026 financial guidance?

Vericel raised full-year revenue guidance to $344 million to $346 million from $330 million to $340 million. It also raised MACI guidance to $290 million to $292 million, Burn Care guidance to $54 million from $46 million to $50 million, and adjusted EBITDA margin guidance to 28% from 27%.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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0000887359false00008873592026-11-052026-11-05

UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549

FORM 8-K

CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

Date of Report (Date of Earliest Event Reported): November 5, 2026

Vericel Corporation
(Exact name of registrant as specified in its charter)
Michigan
001-35280
94-3096597
(State or other jurisdiction of (Commission File Number)(I.R.S. Employer Identification No.)
incorporation)
25 Blue Sky Drive
Burlington,
MA
01803
(Address of principal executive offices)
(Zip Code)

Registrant's telephone number, including area code: (617) 588-5555

Not Applicable
Former name or former address, if changed since last report

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):


☐    Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐    Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐    Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐     Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading Symbol(s)Name of each exchange on which registered
Common Stock, no par valueVCELNASDAQ

Indicate by a check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§240.12b-2 of this chapter). 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. o



Item 2.02. Results of Operations and Financial Condition

On November 5, 2026, Vericel Corporation issued a press release announcing its financial results for the fiscal quarter ended September 30, 2026, a copy of which is attached hereto as Exhibit 99.1 and is incorporated herein by reference.
The information in this Report on Form 8-K and Exhibit 99.1 attached hereto is intended to be furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific reference in such filing.

Item 9.01. Financial Statements and Exhibits
Exhibit No.Description
99.1
Press Release of Vericel Corporation, "Vericel Reports Third Quarter 2026 Financial Results and Raises Full-Year Financial Guidance"
104
Cover page interactive data file (embedded within the Inline XBRL document)




EXHIBIT INDEX
 
Exhibit No.Description
99.1
Press Release of Vericel Corporation, "Vericel Reports Third Quarter 2026 Financial Results and Raises Full-Year Financial Guidance"
104
Cover page interactive data file (embedded within the Inline XBRL document)


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
Vericel Corporation
Date: November 5, 2026
By:/s/ Joseph A. Mara
Name: Joseph A. Mara
Chief Financial Officer
(Principal Financial Officer)




Exhibit 99.1
vericellogoa26a.jpg
Vericel Corporation
25 Blue Sky Drive Burlington, MA 01803
T 617 588-5555 F 617 588-5554
www.vcel.com


Vericel Reports Third Quarter 2026 Financial Results and Raises Full-Year Financial Guidance
Total Revenue Growth of 26% to $85.4 Million
Net Income Increased 179% to $14.2 Million
Adjusted EBITDA Margin of 30%
Raised Full-Year Revenue Guidance to $344 to $346 Million and Adjusted EBITDA Margin Guidance to 28%
Conference Call Today at 8:30am Eastern Time

BURLINGTON, Mass., November 5, 2026 (GLOBE NEWSWIRE) — Vericel Corporation (NASDAQ:VCEL), a leader in advanced therapies for the sports medicine and severe burn care markets, today reported financial results and business highlights for the third quarter ended September 30, 2026.

Third Quarter 2026 Financial Highlights
•Total net revenue growth of 26% to $85.4 million
•MACI® net revenue growth of 21% to $67.4 million
•Burn Care net revenue growth of 52% to $18.0 million, with Epicel® revenue of $12.7 million and NexoBrid® revenue of $5.3 million
•Gross margin of 73%
•Net income increased 179% to $14.2 million, or $0.27 per diluted share
•Non-GAAP adjusted EBITDA increased 48% to $25.2 million, or 30% of revenue
•Operating cash flow of $17.7 million
•Free cash flow of $15.7 million
•$235.6 million in cash and investments, and no debt

Year-to-Date 2026 Financial Highlights
•Total net revenue growth of 26% to $231.3 million
•MACI net revenue growth of 22% to $189.3 million
•Burn Care net revenue growth of 50% to $42.0 million
•Adjusted EBITDA growth of 48% to $49.6 million
•Operating cash flow of $50.3 million
•Free cash flow of $45.1 million
1

Exhibit 99.1

Business Highlights and Updates
•Record third quarter total revenue and MACI revenue, and the highest quarterly Burn Care revenue to date
•MACI revenue growth of 20% or more for the sixth consecutive quarter
•Highest Epicel quarterly revenue since launch, which increased 23% versus the prior year
•Highest NexoBrid quarterly commercial revenue since launch, with 54% growth versus the prior year and 46% growth versus the prior quarter
•Recognized $3.0 million of BARDA procurement revenue in the third quarter
•Record third quarter MACI biopsies, implants and biopsy and implanting surgeons, with biopsy growth increasing each quarter this year compared to the prior year
•Highest number of MACI Arthro cases in any quarter since launch in the third quarter
•The Company remains on track for a potential MACI launch in the U.K. in 2027
•Repurchased 220,744 shares of common stock for $8.8 million during the quarter, with $191.2 million of share repurchase authorization remaining as of September 30, 2026

“The Company delivered outstanding financial and business results in the third quarter as we continue to generate top-tier revenue and profit growth as well as significant free cash flow, while also returning capital to shareholders,” said Nick Colangelo, President and CEO of Vericel. “Given our third quarter outperformance and the strong start to the fourth quarter for both commercial businesses, and particularly for MACI, we believe that the Company is very well-positioned for a strong close to 2026 and to sustain this momentum in 2027 and beyond.”

2026 Full-Year Financial Guidance
•Raised total revenue guidance to $344 to $346 million, compared to $330 to $340 million previously
•Raised MACI revenue guidance to $290 to $292 million, compared to $284 to $290 million previously
•Raised Burn Care revenue guidance to $54 million, compared to $46 to $50 million previously
•Raised adjusted EBITDA margin guidance to 28%, compared to 27% previously
•Reaffirmed full-year gross margin of approximately 75%

Third Quarter 2026 Results
Total net revenue for the quarter ended September 30, 2026 increased 26% to $85.4 million, compared to $67.5 million in the third quarter of 2025. Total net product revenue for the quarter included $67.4 million of MACI (autologous cultured chondrocytes on porcine collagen membrane) net revenue, $12.7 million of Epicel (cultured epidermal autografts) net revenue, $2.3 million of NexoBrid (anacaulase-bcdb) commercial net revenue and $3.0 million of NexoBrid BARDA procurement revenue, compared to $55.7 million of MACI net revenue, $10.4 million of Epicel net revenue, and $1.5 million of commercial NexoBrid net revenue, respectively, in the third quarter of 2025.

2

Exhibit 99.1
Gross profit for the quarter ended September 30, 2026 was $62.6 million, or 73% of net revenue, compared to $49.6 million, or 73% of net revenue, for the third quarter of 2025.

Total operating expenses for the quarter ended September 30, 2026 were $50.4 million, compared to $46.1 million for the same period in 2025. The increase in operating expenses was primarily due to increased headcount and related employee expenses, including the MACI sales force expansion, and an increase in marketing programs.

Net income for the quarter ended September 30, 2026 was $14.2 million, or $0.27 per diluted share, compared to $5.1 million, or $0.10 per diluted share, for the third quarter of 2025.

Non-GAAP adjusted EBITDA for the quarter ended September 30, 2026 was $25.2 million, or 30% of net revenue, compared to $17.0 million, or 25% of net revenue, for the third quarter of 2025. A table reconciling non-GAAP measures is included in this press release for reference.

Conference Call Information
Today’s conference call will be available live at 8:30 a.m. Eastern Time. The live webcast can be accessed on the Investor Relations section of the Vericel website at http://investors.vcel.com/events-presentations. Presentation slides for the conference call will be available on the webcast and on the Vericel website. A replay of the webcast will be available until November 5, 2027.

To participate by telephone, dial 800-330-6730 or +1-312-471-1351 if connecting from outside the U.S. When connecting, please use passcode: 787594.

About Vericel Corporation
Vericel is a leading provider of advanced therapies for the sports medicine and severe burn care markets. The Company combines innovations in biology with medical technologies, resulting in a highly differentiated portfolio of innovative cell therapies and specialty biologics that repair injuries and restore lives. Vericel markets three products in the United States. MACI (autologous cultured chondrocytes on porcine collagen membrane) is an autologous cellularized scaffold product indicated for the repair of symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults. Epicel (cultured epidermal autografts) is a permanent skin replacement for the treatment of patients with deep dermal or full thickness burns greater than or equal to 30% of total body surface area. Vericel also holds an exclusive license for North American rights to NexoBrid (anacaulase-bcdb), a biological orphan product containing proteolytic enzymes, which is indicated for eschar removal in adults and pediatric patients with deep partial-thickness and/or full-thickness thermal burns. For more information, please visit www.vcel.com.

Epicel®, MACI® and MACI Arthro® are registered trademarks of Vericel Corporation. NexoBrid® is a registered trademark of MediWound Ltd. and is used under license to Vericel Corporation. © 2026 Vericel Corporation. All rights reserved.

3

Exhibit 99.1
GAAP v. Non-GAAP Measures
Vericel’s reported earnings are prepared in accordance with generally accepted accounting principles in the United States, or GAAP, and represent earnings as reported to the Securities and Exchange Commission (SEC). Vericel has provided in this release certain financial information that has not been prepared in accordance with GAAP. Vericel’s management believes that the non-GAAP adjusted EBITDA, which includes adjustments for specific items that are generally not indicative of our core operations, and free cash flow described in this release, provide additional information that is useful to investors in understanding Vericel’s underlying performance, business and performance trends, and helps facilitate period-to-period comparisons and comparisons of its financial measures with other companies in Vericel’s industry. However, the non-GAAP financial measures that Vericel uses may differ from measures that other companies may use. Non-GAAP financial measures are not required to be uniformly applied, are not audited and should not be considered in isolation or as substitutes for results prepared in accordance with GAAP.

Forward-Looking Statements
Vericel cautions you that all statements other than statements of historical fact included in this press release that address activities, events or developments that we expect, believe or anticipate will or may occur in the future are forward-looking statements. Although we believe that we have a reasonable basis for the forward-looking statements contained herein, they are based on current expectations about future events affecting us and are subject to risks, assumptions, uncertainties and factors relating to our operations and business environment, all of which are difficult to predict and many of which are beyond our control. Our actual results may differ materially from those expressed or implied by the forward-looking statements in this press release. These statements are often, but are not always, made through the use of words or phrases such as “anticipates,” “intends,” “estimates,” “plans,” “expects,” “continues,” “believe,” “guidance,” “outlook,” “target,” “future,” “potential,” “goals” and similar words or phrases, or future or conditional verbs such as “will,” “would,” “should,” “could,” “may,” or similar expressions.

Among the factors that could cause actual results to differ materially from those set forth in the forward-looking statements include, but are not limited to, uncertainties associated with our expectations regarding future revenue, growth in revenue, market penetration for MACI, MACI Arthro, Epicel, and NexoBrid in the U.S. and in applicable markets outside the U.S., growth in profit, gross margins and operating margins, the ability to continue to scale our manufacturing operations to meet the demand for our cell therapy products, the ability to sustain profitability, the expected target surgeon audience, potential fluctuations in sales and volumes and our results of operations over the course of the year, timing and conduct of clinical trial and product development activities, timing and likelihood of the FDA’s potential approval of the use of MACI to treat cartilage defects in the ankle, the timing and likelihood of obtaining marketing approval for MACI in the United Kingdom, the estimate of the commercial growth potential of our products and product candidates, competitive developments, changes in third-party coverage and reimbursement, including recent and future healthcare and drug pricing reform measures and private payor initiatives, surgeon adoption of MACI Arthro, physician and burn center
4

Exhibit 99.1
adoption of NexoBrid, labor strikes, supply chain disruptions or other events or factors that might affect our ability to manufacture MACI or Epicel or affect MediWound’s ability to manufacture and supply sufficient quantities of NexoBrid to meet customer demand, including but not limited to conflicts in the Middle East region involving Israel or those related to disruptions of land or sea transportation routes or distribution or shipping channels, uncertainties associated with the potential benefits of the Company’s agreement with BARDA for the procurement and development of NexoBrid and the availability of funding from BARDA under that agreement, negative impacts on the global economy and capital markets resulting from the conflicts in Ukraine and Iran, as well as other hostilities in the Middle East, changes in trade policies and regulations, including the potential for increases or changes in duties, current and potentially new tariffs or quotas, lingering effects of adverse developments affecting financial institutions, companies in the financial services industry or the financial services industry generally, changes in governmental monetary and fiscal policies, including, but not limited to, Federal Reserve policies in connection with continued inflationary pressures, the impact from future regulatory, judicial and legislative changes affecting our industry or the broader market, including those included in the One Big Beautiful Bill Act, and a U.S. government shutdown.

These and other significant factors are discussed in greater detail in Vericel’s Annual Report on Form 10-K for the year ended December 31, 2025, filed with the SEC on February 26, 2026, Vericel’s Quarterly Report on Form 10-Q for the quarter ended September 30, 2026, filed with the SEC on November 5, 2026, and in other filings with the SEC. These forward-looking statements reflect our views as of the date hereof and Vericel does not assume and specifically disclaims any obligation to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date of this release except as required by law.

Investor Contact:
Eric Burns
ir@vcel.com
+1 (734) 418-4411


5

Exhibit 99.1

VERICEL CORPORATION
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(in thousands, except per share amounts - unaudited)

Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Product sales, net$85,371 $67,503 $231,253 $183,341 
Total revenue85,371 67,503 231,253 183,341 
Cost of product sales22,761 17,918 62,975 50,870 
Gross profit62,610 49,585 168,278 132,471 
Research and development6,885 6,318 22,482 20,310 
Selling, general and administrative43,539 39,817 141,240 123,532 
Total operating expenses50,424 46,135 163,722 143,842 
Income (loss) from operations12,186 3,450 4,556 (11,371)
Other income (expense):
Interest income2,152 1,808 5,957 5,122 
Interest expense(160)(158)(480)(468)
Other (expense) income(17)(26)32 (8)
Total other income1,975 1,624 5,509 4,646 
Net income (loss)$14,161 $5,074 $10,065 $(6,725)
Net income (loss) per common share:
Basic$0.28 $0.10 $0.20 $(0.13)
Diluted$0.27 $0.10 $0.19 $(0.13)
Weighted-average common shares outstanding:
Basic51,186 50,489 51,013 50,256 
Diluted52,962 51,908 52,459 50,256 

6

Exhibit 99.1
VERICEL CORPORATION
RECONCILIATION OF REPORTED NET INCOME (LOSS) (GAAP)
TO ADJUSTED EBITDA (NON-GAAP MEASURE)
(in thousands - unaudited)

Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Net income (loss)$14,161 $5,074 $10,065 $(6,725)
Stock-based compensation expense7,823 8,699 28,200 30,344 
Depreciation and amortization3,627 2,944 10,514 8,456 
Net interest income(1,992)(1,654)(5,485)(4,658)
Pre-occupancy lease expense and tech transfer1,604 1,933 6,349 6,180 
Adjusted EBITDA (Non-GAAP)$25,223 $16,996 $49,643 $33,597 


7

Exhibit 99.1
VERICEL CORPORATION
RECONCILIATION OF FREE CASH FLOW (NON-GAAP MEASURE)
(in thousands - unaudited)

Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Net cash provided by operating activities$17,723 $22,082 $50,297 $36,896 
Capital expenditures(2,042)(2,630)(5,231)(24,975)
Free cash flow (Non-GAAP)$15,681 $19,452 $45,066 $11,921 
Net cash used in investing activities$(2,708)$(3,377)$(9,729)$(27,547)
Net cash (used in) provided by financing activities$(6,880)$1,166 $(7,167)$6,005 
8

Exhibit 99.1
VERICEL CORPORATION
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands - unaudited)

September 30,December 31,
20262025
ASSETS
Current assets:
Cash and cash equivalents$133,493 $100,092 
Short-term investments36,775 37,407 
Accounts receivable (net of allowance for doubtful accounts of $23 and $13, respectively)81,798 84,634 
Inventory17,056 17,560 
Other current assets11,648 7,744 
Total current assets280,770 247,437 
Property and equipment, net105,079 108,397 
Intangible assets, net5,156 5,625 
Right-of-use assets60,590 64,774 
Long-term investments65,336 61,395 
Other long-term assets179 341 
Total assets$517,110 $487,969 
LIABILITIES AND SHAREHOLDERS’ EQUITY
Current liabilities:
Accounts payable$19,958 $15,828 
Accrued expenses20,391 19,236 
Current portion of operating lease liabilities14,254 13,969 
Other current liabilities116 116 
Total current liabilities54,719 49,149 
Operating lease liabilities76,319 82,284 
Other long-term liabilities1,900 1,896 
Total liabilities132,938 133,329 
Total shareholders’ equity384,172 354,640 
Total liabilities and shareholders’ equity$517,110 $487,969 

9

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