STOCK TITAN

Ceribell raises 2026 revenue outlook to $115M–$117M

The raised 2026 revenue range represents approximately 29% to 31% growth over 2025 revenue, excluding material contributions from neonate, pediatric and delirium products.

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(High)

Sentiment and the balance of points

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Form Type
8-K

Rhea-AI Filing Summary

Ceribell, Inc. (CBLL) reported third-quarter 2026 revenue of $29.341 million, up 30% from $22.589 million a year earlier. Product revenue was $22.235 million and subscription revenue was $7.106 million. Gross margin was 90%, compared with 88%, while operating expenses increased 36% to $46.888 million. Net loss was $21.351 million, compared with $13.465 million, and adjusted EBITDA loss, a non-GAAP measure, was $12.140 million versus $9.230 million.

At quarter-end, Ceribell had 747 active accounts and added 35 net new customers; same-store utilization grew by double digits. The company received FDA 510(k) clearance for Quantitative EEG Trending and Amplitude-Integrated EEG Analysis and fully launched its delirium monitoring solution after a commercial pilot. Cash, cash equivalents and marketable securities totaled $117.5 million as of September 30, 2026. An August credit facility provides access to up to $60 million in committed capital and an additional $25 million in uncommitted capital at the lender’s discretion. Full-year 2026 revenue guidance was raised to $115 million to $117 million, representing approximately 29% to 31% growth over 2025 revenue; the range excludes material contributions from neonate, pediatric or delirium products.

1 point · 0 major

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Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 1 point

How the balance works

Positive

  • Moderate pointThird-quarter revenue rose 30% to $29.341 million year over year.

Negative

  • Moderate pointThird-quarter net loss was $21.351 million, versus $13.465 million a year earlier.

Filing Explained

The balance sheet shows 38,820,703 common shares outstanding at September 30, 2026, versus 37,485,124 at December 31, 2025; with a fixed holding, an existing holder owns a smaller fraction of the share base.

Item 2.02 Results of Operations and Financial Condition Financial
Disclosure of earnings results, typically an earnings press release or preliminary financials.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, or exhibit attachments filed with this report.
Third-quarter revenue $29.341 million Three months ended September 30, 2026
Year-over-year revenue growth 30% Third quarter 2026 compared with third quarter 2025
Net loss $21.351 million Three months ended September 30, 2026
Adjusted EBITDA loss (non-GAAP) $12.140 million Three months ended September 30, 2026
Gross margin 90% Third quarter 2026; 88% in third quarter 2025
Full-year revenue guidance $115 million to $117 million 2026; approximately 29% to 31% growth over 2025 revenue
Cash, cash equivalents and marketable securities $117.5 million As of September 30, 2026
Credit facility capital Up to $60 million committed; $25 million uncommitted Entered into in August 2026; uncommitted capital available at the lender’s discretion
Adjusted EBITDA financial
"Adjusted EBITDA loss (a non-GAAP measure)"
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.
same-store utilization financial
"double-digit year-over-year same-store utilization growth"
510(k) clearance regulatory
"Received U.S. Food and Drug Administration 510(k) clearance"
A 510(k) clearance is a U.S. regulatory approval that lets a medical device be sold because it is shown to be substantially similar to an already-legal device; think of it as a passport saying the new product is close enough to a known item to enter the market without a full, lengthy review. For investors, 510(k) clearance signals faster, lower-cost market access and reduced regulatory risk compared with new, untested device pathways, which can materially affect timelines, costs and revenue prospects.
electroencephalography technical
"electroencephalography (“EEG”) platform"
Electroencephalography is a medical test that uses small sensors on the scalp to record the brain’s electrical activity over time, like an EKG for the brain. Investors care because EEG data can be used in drug and device development, patient diagnosis, and monitoring treatment effects; strong EEG results can influence clinical success, regulatory approvals, and market adoption, affecting a company’s value and risk profile.
Total revenue $29.341 million +30% year over year
Net loss $21.351 million Compared with $13.465 million in third quarter 2025
Adjusted EBITDA loss (non-GAAP) $12.140 million Compared with $9.230 million in third quarter 2025
Gross margin 90% Compared with 88% in third quarter 2025
Guidance

Raised full-year 2026 revenue guidance to $115 million to $117 million, representing approximately 29% to 31% growth over 2025 revenue; excludes material contributions from neonate, pediatric or delirium products.

FAQ

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

How much revenue did CBLL report in the third quarter of 2026?

Ceribell reported $29.341 million in third-quarter revenue, a 30% increase from $22.589 million in the third quarter of 2025. Product revenue was $22.235 million, and subscription revenue was $7.106 million.

What is CBLL's 2026 revenue guidance?

Ceribell raised its full-year 2026 revenue guidance to $115 million to $117 million, representing approximately 29% to 31% growth over 2025 revenue. The range excludes material contributions from neonate, pediatric or delirium products.

What does Ceribell's credit facility include?

Entered into in August 2026, the facility provides access to up to $60 million in committed capital: a $30 million term loan and a $30 million revolving credit facility. It also includes $25 million of uncommitted capital available at the lender’s discretion.

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

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0001861107false00018611072026-11-032026-11-03

 

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 3, 2026

CeriBell, Inc.

(Exact name of registrant as specified in its charter)

 

 

 

 

 

Delaware

001-42364

47-1785452

(State or other jurisdiction

of incorporation)

(Commission

File Number)

(IRS Employer

Identification Number)

 

 

 

 

 

360 N. Pastoria Avenue

Sunnyvale, California

 

 

 

 

94085

(Address of principal executive offices)

 

 

 

(Zip Code)

Registrant’s telephone number, including area code: (800) 436-0826

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:

☐

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 class

Trading Symbol(s)

Name of each exchange on which registered

Common Stock, $0.001 par value per share

CBLL

The Nasdaq Stock Market LLC

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§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. ☐

 


 

Item 2.02

Results of Operations and Financial Condition.

On November 3, 2026, CeriBell, Inc. issued a press release announcing its financial results for the fiscal quarter ended September 30, 2026. A copy of the press release, dated November 3, 2026, is furnished hereto as Exhibit 99.1 and is incorporated herein by reference.

The foregoing information in this Item 2.02 (including Exhibit 99.1) shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, except as shall be expressly set forth by specific reference in such filing.

 

Item 9.01

Financial Statements and Exhibits.

 

Exhibit No.

Description

99.1

Press Release of CeriBell, Inc., dated November 3, 2026.

104

Cover Page Interactive Data File, formatted in Inline XBRL.

 

 


 

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

 

 

 

 

 

 

 

 

CERIBELL, INC.

 

 

 

 

Date: November 3, 2026

 

By:

/s/ Scott Blumberg

 

 

 

Scott Blumberg

 

 

 

Chief Financial Officer

 

 


 

img260468198_0.jpg

 

Ceribell Reports Third Quarter 2026 Financial Results

 

Sunnyvale, Calif. – November 3, 2026 – CeriBell, Inc. (Nasdaq: CBLL) (“Ceribell”), a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions, today reported financial results for the third quarter ended September 30, 2026.

 

Third Quarter 2026 & Recent Highlights

•
Reported total revenue of $29.3 million in the third quarter of 2026, a 30% increase compared to the same period in 2025
•
Ended the quarter with 747 total active accounts, adding a record 35 net new customers in the quarter
•
Drove double-digit year-over-year same-store utilization growth
•
Achieved gross margin of 90%
•
Announced the full launch of the Company’s delirium monitoring solution following the conclusion of its successful commercial pilot
•
Received U.S. Food and Drug Administration 510(k) clearance for Quantitative EEG Trending and Amplitude-Integrated EEG Analysis

 

“Our third quarter results reflect new highs in account additions and utilization within our existing account base, demonstrating the strength of our core seizure business as a durable growth engine,” said co-founder and CEO Jane Chao, Ph.D. “With the full launch of our delirium monitoring solution and the coming introduction of our new hardware platform, we are well positioned for a pivotal 2027 as we advance our mission to establish EEG as a new vital sign.”

 

Third Quarter 2026 Financial Results

Total revenue in the third quarter of 2026 was $29.3 million, a 30% increase from $22.6 million in the third quarter of 2025. The increase was primarily driven by the success of the Company’s same-store growth strategy, which delivered record utilization within its existing account base, in addition to increased adoption of the Ceribell System across new and existing accounts. Product revenue for the third quarter of 2026 was $22.2 million, representing an increase of 31% from $17.0 million in the third quarter of 2025. Subscription revenue for the third quarter of 2026 was $7.1 million, representing an increase of 28% from $5.6 million in the third quarter of 2025, reflecting continued growth in the Company’s installed base of Clarity subscriptions.

Gross profit in the third quarter of 2026 was $26.3 million, compared to $19.9 million for the third quarter of 2025. Gross margin for the third quarter of 2026 was 90%, compared to 88% for the same period in 2025. Gross margin strength was driven by manufacturing cost reduction initiatives and the impact of the Company’s introduction of a fully operational manufacturing line in Vietnam.

Operating expenses in the third quarter of 2026 were $46.9 million, compared to $34.6 million for the third quarter of 2025, representing an increase of 36%. The increase in operating expenses was primarily attributable to continued investments in the Company’s commercial organization, including infrastructure in advance of the delirium launch, investments in research and development to support its next-generation hardware platform, algorithm development and clinical studies, stock-based compensation expense, and legal costs associated with intellectual property enforcement activities.

 


 

Net loss in the third quarter of 2026 was $21.4 million, or $0.55 net loss per share, compared to a net loss of $13.5 million, or $0.37 net loss per share, for the same period in 2025.

 

Adjusted EBITDA loss (a non-GAAP measure) for the third quarter of 2026 was $12.1 million, compared to $9.2 million in the third quarter of 2025. Reconciliations of EBITDA and Adjusted EBITDA for the three months ended September 30, 2026 and 2025 are in the financial schedules that are included with this press release.

Cash, cash equivalents, and marketable securities totaled $117.5 million as of September 30, 2026. In August 2026, the Company further strengthened its balance sheet by entering into a new credit facility providing access to up to $60 million in committed capital, comprising a $30 million term loan and a $30 million revolving credit facility, with an additional $25 million of uncommitted capital available at the lender’s discretion.

 

2026 Financial Outlook

Ceribell is raising its revenue guidance for the full year 2026 to a range of $115 million to $117 million, representing growth of approximately 29% to 31% over the Company’s prior year revenue. This update reflects the Company’s continued momentum in its core business, driven by both new account additions and increased utilization within its established account base. The updated range does not include material contributions from the Company’s neonate, pediatric, or delirium products.

 

Webcast and Conference Call Details

Ceribell will host a conference call today, November 3, 2026, at 1:30 p.m. PT / 4:30 p.m. ET to discuss its third quarter 2026 financial results. Investors interested in listening to the conference call may do so by dialing (800) 715-9871 for domestic callers or (646) 307-1963 for international callers and providing access code 1880547. A live and archived webcast of the event will be available on the “Investor Relations” section of the Ceribell website at https://investors.ceribell.com/.

Forward-Looking Statements

Except where otherwise noted, the information contained in this earnings release and the related attachments is as of November 3, 2026. We assume no obligation to update any forward-looking statements contained in this earnings release and the related attachments as a result of new information or future events or developments. This earnings release and the related attachments contain forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including statements about, among other topics, our anticipated operating and financial performance, including financial guidance and projections; business plans, strategy, goals and prospects; and expectations for our products. Given their forward-looking nature, these statements involve substantial risks, uncertainties, and assumptions, and we cannot ensure that any outcome expressed in these forward-looking statements will be realized in whole or in part. You can identify these statements by the fact that they use future dates or use words such as “will,” “may,” “could,” “likely,” “ongoing,” “anticipate,” “estimate,” “expect,” “project,” “intend,” “plan,” “believe,” “assume,” “target,” “forecast,” “guidance,” “goal,” “objective,” “aim,” “seek,” “potential,” “hope,” and other words and terms of similar meaning. Our financial guidance is based on estimates and assumptions that are subject to significant uncertainties. Among the factors that could cause actual results to differ materially from past results and future plans and projected future results are the following: risks related to our limited operating history and history of net losses; our ability to successfully achieve substantial market acceptance and adoption of our products; competitive pressures; our manufacturing operations, including our reliance on third-party manufacturers and suppliers in China and Vietnam and our ability to adapt to evolving demand; product defects or complaints and related liability; the complexity, timing, expense, and outcomes of clinical studies, legal matters, and regulatory compliance; our ability to obtain and maintain adequate coverage and reimbursement levels for our products; our ability to comply with changing laws and regulatory requirements and resulting costs; our dependence on a limited number of suppliers; geopolitical conflicts and related supply chain disruptions; and other risks and uncertainties, including those described under the heading “Risk Factors” in our most recent Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q, as well as in other reports filed with the U.S. Securities and Exchange Commission (“SEC”). These filings, when made, are available on the Investor Relations section of our website at https://investors.ceribell.com/ and on the SEC’s website at https://sec.gov/.

 


 

 

Non-GAAP Financial Measures

EBITDA and Adjusted EBITDA are non-GAAP financial measures. Ceribell defines EBITDA as GAAP net loss adjusted to exclude (i) provision for income taxes, (ii) depreciation and amortization expense, and (iii) interest income and interest expense, net. EBITDA is then adjusted to exclude (iv) stock-based compensation expense, (v) legal fees and related professional services costs incurred in connection with the patent infringement action we filed against Natus Medical Incorporated and certain of its subsidiaries in July 2025, as further described in Part II, Item 1 — Legal Proceedings of Ceribell's Quarterly Report on Form 10-Q, and (vi) the loss on debt extinguishment to arrive at Adjusted EBITDA. Management uses EBITDA and Adjusted EBITDA to evaluate ongoing operations and for internal planning and forecasting purposes. Ceribell believes EBITDA and Adjusted EBITDA provide investors with meaningful supplemental information regarding its performance by excluding certain items that may not be indicative of its business, results of operations, or outlook. EBITDA and Adjusted EBITDA should not be considered in isolation, as a substitute for, or superior to GAAP net loss, and may not be comparable to similarly titled measures used by other companies. Reconciliations between U.S. GAAP and non-GAAP results are presented in the accompanying tables of this release.

About CeriBell, Inc.

Ceribell is a medical technology company focused on transforming the diagnosis and management of patients with serious neurological conditions. Ceribell has developed the Ceribell System, a novel point-of-care electroencephalography (“EEG”) platform specifically designed to address the unmet needs of patients in the acute-care setting. By combining proprietary, highly portable, and rapidly deployable hardware with sophisticated artificial intelligence (“AI”)-powered algorithms, the Ceribell System enables rapid diagnosis and continuous monitoring of patients with neurological conditions. The Ceribell System is FDA-cleared for use in detecting seizure and monitoring delirium in intensive care units and emergency rooms across the U.S. Ceribell is headquartered in Sunnyvale, California. For more information, please visit https://www.ceribell.com or follow the company on LinkedIn.

Investor Contacts

Brian Johnston

Gilmartin Group

Investors@ceribell.com

Media Contact

Laura Hartlieb

Press@ceribell.com

 


 

 

CeriBell, Inc.

Condensed Statements of Operations and Comprehensive Loss

(in thousands, except share and per share data)

(unaudited)

 

 

 

Three months ended September 30,

 

 

Nine months ended September 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Revenue

 

 

 

 

 

 

 

 

 

 

 

 

Product revenue

 

$

22,235

 

 

$

17,020

 

 

$

63,667

 

 

$

48,551

 

Subscription revenue

 

 

7,106

 

 

 

5,569

 

 

 

20,266

 

 

 

15,728

 

Total revenue

 

 

29,341

 

 

 

22,589

 

 

 

83,933

 

 

 

64,279

 

Cost of revenue

 

 

 

 

 

 

 

 

 

 

 

 

Product cost of goods sold

 

 

2,658

 

 

 

2,461

 

 

 

7,557

 

 

 

7,172

 

Subscription cost of revenue

 

 

343

 

 

 

186

 

 

 

976

 

 

 

476

 

Total cost of revenue

 

 

3,001

 

 

 

2,647

 

 

 

8,533

 

 

 

7,648

 

Gross profit

 

 

26,340

 

 

 

19,942

 

 

 

75,400

 

 

 

56,631

 

Operating expenses

 

 

 

 

 

 

 

 

 

 

 

 

Research and development

 

 

7,403

 

 

 

4,983

 

 

 

20,311

 

 

 

14,081

 

Sales and marketing

 

 

25,032

 

 

 

18,569

 

 

 

71,837

 

 

 

54,024

 

General and administrative

 

 

14,453

 

 

 

11,037

 

 

 

44,526

 

 

 

32,332

 

Total operating expenses

 

 

46,888

 

 

 

34,589

 

 

 

136,674

 

 

 

100,437

 

Loss from operations

 

 

(20,548

)

 

 

(14,647

)

 

 

(61,274

)

 

 

(43,806

)

Interest expense

 

 

(267

)

 

 

(480

)

 

 

(1,139

)

 

 

(1,428

)

Other income (expense), net

 

 

(536

)

 

 

1,662

 

 

 

2,056

 

 

 

5,349

 

Loss before provision for income taxes

 

 

(21,351

)

 

 

(13,465

)

 

 

(60,357

)

 

 

(39,885

)

Provision for income tax expense

 

 

—

 

 

 

—

 

 

 

—

 

 

 

—

 

Net loss

 

$

(21,351

)

 

$

(13,465

)

 

$

(60,357

)

 

$

(39,885

)

Net loss per share attributable to common stockholders:

 

 

 

 

 

 

 

 

 

 

 

 

Basic and diluted

 

 

(0.55

)

 

 

(0.37

)

 

 

(1.59

)

 

 

(1.10

)

Weighted-average shares used in computing net loss per share attributable to common stockholders:

 

 

 

 

 

 

 

 

 

 

 

 

Basic and diluted

 

 

38,500,027

 

 

 

36,806,918

 

 

 

38,068,145

 

 

 

36,326,792

 

Other comprehensive loss

 

 

 

 

 

 

 

 

 

 

 

 

Net unrealized gain (loss) on marketable securities

 

$

(51

)

 

$

134

 

 

$

(302

)

 

$

139

 

Comprehensive loss

 

$

(21,402

)

 

$

(13,331

)

 

$

(60,659

)

 

$

(39,746

)

 

 


 

CeriBell, Inc.

Condensed Balance Sheets

(in thousands, except share and per share data)

(unaudited)

 

 

 

September 30,

 

 

December 31,

 

 

 

2026

 

 

2025

 

Assets

 

 

 

 

 

 

Current assets

 

 

 

 

 

 

Cash and cash equivalents

 

$

41,989

 

 

$

40,476

 

Marketable securities

 

 

75,478

 

 

 

118,785

 

Accounts receivable, net

 

 

17,792

 

 

 

15,053

 

Inventory

 

 

6,955

 

 

 

7,288

 

Contract costs, current

 

 

2,232

 

 

 

2,210

 

Prepaid expenses and other current assets

 

 

2,991

 

 

 

2,906

 

Total current assets

 

 

147,437

 

 

 

186,718

 

Property and equipment, net

 

 

1,774

 

 

 

2,030

 

Operating lease right-of-use assets

 

 

1,516

 

 

 

2,296

 

Contract costs, long-term

 

 

1,503

 

 

 

1,847

 

Other non-current assets

 

 

4,140

 

 

 

2,912

 

Total assets

 

$

156,370

 

 

$

195,803

 

Liabilities and stockholders’ equity

 

 

 

 

 

 

Current liabilities

 

 

 

 

 

 

Accounts payable

 

$

2,334

 

 

$

2,838

 

Accrued liabilities

 

 

14,059

 

 

 

14,328

 

Deferred revenue

 

 

230

 

 

 

—

 

Contract liabilities, current

 

 

—

 

 

101

 

Operating lease liability, current

 

 

1,218

 

 

 

1,105

 

Other current liabilities

 

 

193

 

 

818

 

Total current liabilities

 

 

18,034

 

 

 

19,190

 

Long-term liabilities

 

 

 

 

 

 

Notes payable, long-term

 

 

20,000

 

 

 

19,811

 

Other liabilities, long-term

 

 

367

 

 

106

 

Operating lease liability, long-term

 

 

432

 

 

 

1,360

 

Total long-term liabilities

 

 

20,799

 

 

 

21,277

 

Total liabilities

 

$

38,833

 

 

$

40,467

 

Commitments and contingencies

 

 

 

 

 

 

Stockholders’ equity

 

 

 

 

 

 

Preferred stock, $0.001 par value;

 

 

 

 

 

 

Authorized shares: 10,000,000 as of September 30, 2026 and December 31, 2025

 

 

 

 

 

 

Issued and outstanding shares: none as of September 30, 2026 and December 31, 2025

 

 

—

 

 

 

—

 

Common stock, $0.001 par value;

 

 

 

 

 

 

Authorized shares: 500,000,000 as of September 30, 2026 and December 31, 2025

 

 

 

 

 

 

Issued and outstanding shares: 38,820,703 and 37,485,124 as of September 30, 2026 and December 31, 2025, respectively

 

 

39

 

 

 

38

 

Additional paid-in capital

 

 

398,353

 

 

 

375,495

 

Accumulated other comprehensive income (loss)

 

 

(143

)

 

 

159

 

Accumulated deficit

 

 

(280,712

)

 

 

(220,356

)

Total stockholders’ equity

 

 

117,537

 

 

 

155,336

 

Total liabilities and stockholders’ equity

 

$

156,370

 

 

$

195,803

 

 

 


 

CeriBell, Inc.

Reconciliation of U.S. GAAP to Non-GAAP Financial Measures

(in thousands)

(unaudited)

 

 

 

Three months ended September 30,

 

 

Nine months ended September 30,

 

 

 

2026

 

 

2025

 

 

2026

 

 

2025

 

Net Loss (GAAP)

 

$

(21,351

)

 

$

(13,465

)

 

$

(60,357

)

 

$

(39,885

)

Non-GAAP Adjustments:

 

 

 

 

 

 

 

 

 

 

 

 

Interest (income) and expense, net

 

 

(759

)

 

 

(1,208

)

 

 

(2,460

)

 

 

(3,948

)

Depreciation and amortization

 

 

249

 

 

 

391

 

 

 

733

 

 

 

1,050

 

EBITDA (Non-GAAP)

 

 

(21,861

)

 

 

(14,282

)

 

 

(62,084

)

 

 

(42,783

)

Stock-based compensation

 

 

7,099

 

 

 

3,349

 

 

 

16,820

 

 

 

8,864

 

IP litigation matter

 

 

1,073

 

 

 

1,703

 

 

 

10,580

 

 

 

3,756

 

Loss on debt extinguishment

 

 

1,549

 

 

 

—

 

 

 

1,549

 

 

 

—

 

Adjusted EBITDA (Non-GAAP)

 

$

(12,140

)

 

$

(9,230

)

 

$

(33,135

)

 

$

(30,163

)

 

 

 


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