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CVRx Reports Fourth Quarter and Full Year 2025 Financial and Operating Results

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CVRx (NASDAQ: CVRX) reported Q4 2025 revenue of $16.0M (+4% YoY) and full-year 2025 revenue of $56.7M (+10% YoY). Gross margin rose to 85% (FY) and active U.S. implanting centers increased to 252.

The company initiated the BENEFIT-HF randomized trial (2,500 patients, CMS Category B IDE) and amended a term loan to an aggregate facility up to $100M, borrowing an additional $10M (outstanding principal $60M). 2026 revenue guidance: $63.0M–$67.0M.

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Positive

  • Full-year revenue +10% to $56.7M
  • Gross margin improved to 85% for 2025
  • Initiated BENEFIT-HF trial: 2,500 patients, CMS Category B IDE
  • Term loan amended to up to $100M; $10M borrowed (outstanding $60M)
  • 2026 revenue guidance of $63.0M–$67.0M

Negative

  • Net loss of $53.3M for 2025 (though improved vs. prior year)
  • Operating expenses expected at $103M–$107M in 2026
  • Net cash used in operations and investing of $40.8M in 2025

Key Figures

Q4 2025 revenue: $16.0M 2025 revenue: $56.7M Q4 2025 gross margin: 86% +5 more
8 metrics
Q4 2025 revenue $16.0M Quarter ended Dec 31, 2025; +4% YoY
2025 revenue $56.7M Full year 2025; +10% YoY
Q4 2025 gross margin 86% Quarter ended Dec 31, 2025; up from 83%
Q4 2025 net loss $11.9M Quarter ended Dec 31, 2025; $0.46 per share
2025 net loss $53.3M Full year 2025; $2.04 per share
Cash & equivalents $75.7M As of Dec 31, 2025
BENEFIT-HF sample size 2,500 patients Planned randomized controlled trial enrollment
BENEFIT-HF net cost $20M–$30M Expected over 5–7 years

Market Reality Check

Price: $5.70 Vol: Volume 218,514 is below t...
low vol
$5.70 Last Close
Volume Volume 218,514 is below the 20-day average of 390,775, suggesting limited pre‑earnings positioning. low
Technical Shares at $6.08 are trading below the $7.71 200-day MA and 60.56% below the 52-week high.

Peers on Argus

CVRX was down 9.12% while peers were mixed: BSGM +39.91%, TLSI +4.58%, but ELMD ...

CVRX was down 9.12% while peers were mixed: BSGM +39.91%, TLSI +4.58%, but ELMD -17.04%, SGHT -4.98%, STIM -3.74%, pointing to company-specific pressure rather than a broad medical-device move.

Previous Earnings Reports

5 past events · Latest: Jan 12 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Jan 12 Prelim 2025 results Positive -9.9% Preliminary Q4 and FY 2025 revenue with 2026 guidance and CPT code update.
Nov 05 Q3 2025 earnings Positive -2.0% Q3 2025 revenue growth, margin expansion, updated full‑year guidance.
Aug 04 Q2 2025 earnings Positive -9.9% Q2 revenue growth, higher U.S. HF revenue, and guidance update despite losses.
May 08 Q1 2025 earnings Positive -38.7% Q1 revenue growth, more implanting centers, updated 2025 guidance and losses.
Apr 07 Prelim Q1 2025 Positive -46.3% Preliminary Q1 revenue, cash update, and ATM issuance details.
Pattern Detected

Earnings-related headlines have historically prompted negative reactions, with an average move of -21.34%, indicating frequent selling around results despite revenue growth.

Recent Company History

Across the last five earnings events from April 2025 through January 2026, CVRx consistently reported double‑digit revenue growth, expanding implanting centers, and high gross margins. However, each earnings or preliminary results release was followed by a negative price reaction, including moves of -38.69% and -46.27%. Today’s full Q4 and 2025 report largely confirms preliminary figures and reiterates 2026 guidance, fitting into a pattern of operational progress alongside weak stock responses.

Historical Comparison

earnings
-21.3 %
Average Historical Move
Historical Analysis

In the past year, five earnings or preliminary earnings releases averaged a -21.34% move. Against that backdrop, today’s -9.12% pre‑announcement decline fits a recurring pattern of selling around CVRX results.

Typical Pattern

Earnings across 2025 showed steadily rising revenue and high gross margins but persistent net losses. Despite operational expansion in implanting centers and sales coverage, each results update was followed by a negative share reaction.

Regulatory & Risk Context

Active S-3 Shelf · $150,000,000
Shelf Active
Active S-3 Shelf Registration 2025-11-06
$150,000,000 registered capacity

An effective Form S-3 shelf filed on Nov 6, 2025 allows CVRx to issue up to $150,000,000 of various securities via future prospectus supplements. One supplement (a $50,000,000 ATM program with Jefferies) has already been used, indicating an established pathway for additional capital raises.

Market Pulse Summary

This announcement details steady top‑line growth, with 2025 revenue of $56.7M and high gross margins...
Analysis

This announcement details steady top‑line growth, with 2025 revenue of $56.7M and high gross margins around 85–86%, alongside a still‑significant net loss of $53.3M. Management reaffirmed 2026 guidance and outlined the large 2,500‑patient BENEFIT-HF trial, expected to cost $20–$30M. Investors may track execution on revenue targets, operating expense control, trial enrollment progress, use of the $150M shelf and ATM program, and debt under the $100M term facility.

Key Terms

category i cpt codes, randomized controlled trial, left ventricular ejection fractions, nt-probnp, +3 more
7 terms
category i cpt codes regulatory
"Category I CPT codes and the related favorable physician fee payment levels took effect"
Category I CPT codes are standardized numeric labels used by doctors and hospitals to describe common medical procedures and services for billing and insurance purposes. Think of them like a universal price tag and barcode for a medical service: having a Category I code makes it easier for providers to bill insurers and for payers to decide coverage, which directly affects how reliably and quickly a procedure generates revenue and is adopted across the health system.
randomized controlled trial medical
"a landmark randomized controlled trial designed to evaluate Barostim's impact"
A randomized controlled trial is a research method that tests the effects of a new idea or treatment by randomly dividing participants into two groups: one that receives the treatment and one that does not. This approach helps ensure that the results are fair and unbiased, providing clear evidence about whether the treatment actually works. Investors value such trials because they offer reliable information that can influence decision-making and reduce uncertainty.
left ventricular ejection fractions medical
"patients with left ventricular ejection fractions up to 50%"
Left ventricular ejection fraction (LVEF) is the percentage of blood the heart’s main pumping chamber pushes out with each beat, like how much water a pump expels from a tank each cycle. Investors care because LVEF is a key measure used by regulators, doctors and trial designers to judge disease severity, treatment need and eligibility for drugs or devices, which affects market size, approval odds and healthcare spending.
nt-probnp medical
"NT-proBNP levels up to 5,000 pg/mL"
A blood test marker released when the heart is under strain; higher NT‑proBNP levels indicate the heart is working harder or may be failing, similar to a dashboard warning light that signals engine stress. Investors watch NT‑proBNP because changes in the marker can drive clinical trial results, treatment approvals, hospital use, and insurance decisions for heart drugs and devices, all of which affect revenue, adoption and valuation in healthcare companies.
at-the-market program financial
"offer and sell shares of its common stock in an at-the-market program"
An at-the-market program is a way for a company to sell new shares of its stock gradually over time directly into the stock market, rather than all at once. This approach allows the company to raise money as needed while giving investors the opportunity to buy shares at current market prices. It helps manage the timing and price of new stock offerings, providing flexibility for both the company and investors.
shelf registration statement regulatory
"filed a shelf registration statement on Form S-3 to offer and sell up to"
A shelf registration statement is a document a company files with regulators that allows it to sell shares or bonds quickly when it’s a good time to raise money. It’s like having a pre-approved plan ready so the company can act fast without going through lengthy paperwork each time they want to sell, making fundraising more flexible.
term loan agreement financial
"amended its term loan agreement with an affiliate of Innovatus Capital Partners"
A term loan agreement is a formal contract in which a borrower receives a fixed amount of money from a lender and agrees to repay it over a set period with interest, much like a mortgage or car loan for a business. It matters to investors because the scheduled repayments, interest cost and any lender-imposed rules affect a company’s cash flow, financial flexibility and creditworthiness, which can change risk and share value.

AI-generated analysis. Not financial advice.

MINNEAPOLIS, Feb. 12, 2026 (GLOBE NEWSWIRE) -- CVRx, Inc. (NASDAQ: CVRX) ("CVRx"), a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases, today announced its financial and operating results for the fourth quarter and full year of 2025.

Recent Highlights

  • Total revenue for the fourth quarter 2025 was $16.0 million, an increase of 4% over the prior year quarter
  • U.S. revenue for the fourth quarter of 2025 was $14.9 million, an increase of 4% over the prior year quarter
  • Total revenue for 2025 was $56.7 million, an increase of 10% over the prior year
  • Active implanting centers in the U.S. grew to 252 in 2025, as compared to 223 in the prior year
  • Initiated the BENEFIT-HF trial with first enrollments expected in the second quarter of 2026
  • Category I CPT codes and the related favorable physician fee payment levels took effect on Jan. 1, 2026

"We achieved key foundational goals in 2025, and we're heading into 2026 with increasing momentum. Our sales team is building experience and becoming more effective, and we're seeing strong support at high-potential centers. Additionally, the new Category I CPT codes, effective January 1st, remove automatic prior authorization denials. Finally, the initiation of the landmark BENEFIT-HF trial under CMS Category B IDE coverage is a major step that could allow us to triple our addressable market,” said Kevin Hykes, President and Chief Executive Officer of CVRx. “We’re confident that these developments will support our accelerated growth and make Barostim therapy more accessible for heart failure patients in the coming year."

Fourth Quarter 2025 Financial and Operating Results

Revenue was $16.0 million for the three months ended December 31, 2025, an increase of $0.7 million, or 4%, over the three months ended December 31, 2024.

Revenue generated in the U.S. was $14.9 million for the three months ended December 31, 2025, an increase of $0.6 million, or 4%, over the three months ended December 31, 2024. Revenue units in the U.S. totaled 478 and 460 for the three months ended December 31, 2025 and 2024, respectively. The increase was primarily driven by continued growth as a result of the expansion into new sales territories and new accounts, as well as increased physician and patient awareness of Barostim.

As of December 31, 2025, the Company had a total of 252 active implanting centers, as compared to 250 as of September 30, 2025. Active implanting centers are customers that have completed at least one commercial HF implant in the last 12 months. The number of sales territories in the U.S. increased by three to a total of 53 during the three months ended December 31, 2025.

Revenue generated in Europe was $1.1 million for the three months ended December 31, 2025, an increase of $0.1 million, or 10%, over the three months ended December 31, 2024. Total revenue units in Europe increased to 49 for the three months ended December 31, 2025 from 41 in the prior year period. The number of sales territories in Europe remained consistent at five for the three months ended December 31, 2025.

Gross profit was $13.8 million for the three months ended December 31, 2025, an increase of $1.1 million, or 8%, over the three months ended December 31, 2024. Gross margin increased to 86% for the three months ended December 31, 2025, compared to 83% for the three months ended December 31, 2024. Gross margin for the three months ended December 31, 2025 was higher due to an increase in the average selling price and a decrease in the cost per unit, primarily resulting from an increase in manufacturing efficiencies.

R&D expenses increased $0.2 million, or 7%, to $3.0 million for the three months ended December 31, 2025 compared to the three months ended December 31, 2024. This change was primarily driven by a $0.3 million increase in compensation expenses, mainly as a result of increased headcount, partially offset by a $0.1 million decrease in clinical study expenses.

SG&A expenses increased $1.8 million, or 9%, to $22.0 million for the three months ended December 31, 2025 compared to the three months ended December 31, 2024. This change was driven by a $1.3 million increase in compensation expenses, mainly as a result of increased headcount, a $0.5 million increase in advertising expense, and a $0.3 million increase in travel expense, partially offset by a $0.3 million decrease in consulting expense.

Interest expense decreased $0.1 million to $1.4 million for the three months ended December 31, 2025 compared to the three months ended December 31, 2024. This decrease was driven by the lower interest rate on the levels of borrowings under the term loan agreement with Innovatus Capital Partners.

Other income, net was $0.7 million for the three months ended December 31, 2025, compared to $1.1 million for the three months ended December 31, 2024. This decrease was primarily driven by less interest income on our interest-bearing accounts.

Net loss was $11.9 million, or $0.46 per share, for the three months ended December 31, 2025, compared to a net loss of $10.7 million, or $0.43 per share, for the three months ended December 31, 2024. Net loss per share was based on 26.2 million weighted average shares outstanding for three months ended December 31, 2025 and 24.7 million weighted average shares outstanding for the three months ended December 31, 2024.

Full Year 2025 Financial and Operating Results

Revenue was $56.7 million for the year ended December 31, 2025, an increase of $5.4 million, or 10%, over the year ended December 31, 2024.

Revenue generated in the U.S. was $51.9 million for the year ended December 31, 2025, an increase of $4.7 million, or 10%, over the year ended December 31, 2024. Revenue units in the U.S. totaled 1,648 and 1,522 for the years ended December 31, 2025 and 2024, respectively.

As of December 31, 2025, the Company had a total of 252 active implanting centers, as compared to 223 as of December 31, 2024. As of December 31, 2025, we had 53 sales territories in the U.S. as compared to 48 sales territories as of December 31, 2024.

Revenue generated in Europe was $4.8 million for the year ended December 31, 2025, an increase of $0.6 million, or 16%, over the year ended December 31, 2024. Total revenue units in Europe increased to 219 for the year ended December 31, 2025, from 204 for the prior year period. The number of sales territories in Europe remained consistent at five for each of the years ended December 31, 2025 and December 31, 2024.

Gross profit was $48.3 million for the year ended December 31, 2025, an increase of $5.4 million, or 13%, over the year ended December 31, 2024. Gross margin increased to 85% for the year ended December 31, 2025 compared to 84% for the year ended December 31, 2024. Gross margin for the year ended December 31, 2025 was higher due to an increase in the average selling price and a decrease in the cost per unit, primarily due to an increase in manufacturing efficiencies.

R&D expenses were $11.1 million for the years ended December 31, 2025 and December 31, 2024, respectively. R&D expense for the year ended December 31, 2025 included a $0.4 million increase in compensation expenses, mainly as a result of increased headcount, offset by a $0.5 million decrease in clinical study expenses.

SG&A expenses decreased $2.8 million, or 3%, to $88.5 million for the year ended December 31, 2025, compared to the year ended December 31, 2024. This change was driven by a $7.9 million decrease in non-cash stock-based compensation expense, a $0.2 million decrease in insurance expenses, and a $0.2 million decrease in bad debt expense, partially offset by a $4.0 million increase in compensation expenses, mainly as a result of increased headcount and a $1.5 million increase in travel expenses. Approximately $8.4 million of the decrease in non-cash stock-based compensation expense is related to the modification of stock options held by our former Chief Executive Officer in connection with his retirement in the first quarter of 2024.

Interest expense increased $1.4 million to $5.8 million for the year ended December 31, 2025, compared to the year ended December 31, 2024. This increase was driven by the interest expense on borrowings under the term loan agreement with Innovatus Capital Partners.

Other income, net was $3.8 million for the year ended December 31, 2025, compared to $4.0 million for the year ended December 31, 2024. This decrease was primarily driven by less interest income on our interest-bearing accounts.

Net loss was $53.3 million, or $2.04 per share, for the year ended December 31, 2025, compared to a net loss of $60.0 million, or $2.65 per share, for the year ended December 31, 2024. Net loss per share was based on 26.1 million weighted average shares outstanding for year ended December 31, 2025 and 22.6 million weighted average shares outstanding for the year ended December 31, 2024.

As of December 31, 2025, cash and cash equivalents were $75.7 million. Net cash used in operating and investing activities was $40.8 million for the year ended December 31, 2025, compared to $40.5 million for the year ended December 31, 2024.

BENEFIT-HF Clinical Trial

In January 2026, the Company announced the initiation of the BENEFIT-HF trial, a landmark randomized controlled trial designed to evaluate Barostim's impact on all-cause mortality and heart failure decompensation events in an expanded population of heart failure patients with left ventricular ejection fractions up to 50% and NT-proBNP levels up to 5,000 pg/mL. If successful, the BENEFIT-HF trial could expand the indicated patient population for Barostim approximately three times, significantly broadening access to this proven neuromodulation-based approach to heart failure management. The trial is expected to be one of the largest therapeutic cardiac device trials ever performed in heart failure, randomizing 2,500 patients at approximately 150 centers across the U.S. and Germany. The Centers for Medicare & Medicaid Services ("CMS") has approved Category B IDE coverage for the trial, and enrollment is expected to begin in the second quarter of 2026. The net trial costs are expected to be $20 million to $30 million spread over the next five to seven years.

Debt Facility

On January 9, 2026, the Company amended its term loan agreement with an affiliate of Innovatus Capital Partners, LLC, to increase the existing facility by $50 million, to an aggregate principal amount of up to $100 million, subject to the Company’s achievement of certain milestones. Also on the closing date, the Company borrowed an additional $10 million under the term loan agreement, bringing the total outstanding principal amount of term loans to $60 million. The initial interest rate under the amended term loan agreement is equal to the greater of 9.40% or prime plus 2.65%. The interest-only period is extended four years from the closing date and is extendable to five years from the closing date upon achieving certain revenue milestones. The term loans mature in May 2031 and continue to be secured by substantially all of the Company’s assets.

Business Outlook

For the full year of 2026, the Company continues to expect:

  • Total revenue between $63.0 million and $67.0 million;
  • Gross margin between 84% and 86%;
  • Operating expenses between $103.0 million and $107.0 million.

For the first quarter of 2026, the Company expects to report total revenue between $13.7 million and $14.7 million.

Webcast and Conference Call Information

The Company will host a conference call to review its results at 4:30 p.m. Eastern Time today. A live webcast of the investor conference call will be available online at the investor relations page of the Company’s website at ir.cvrx.com. To listen to the conference call on your telephone, please dial 1-877-704-4453 for U.S. callers, or 1-201-389-0920 for international callers, approximately ten minutes prior to the start time.

About CVRx, Inc.

CVRx is a commercial-stage medical device company focused on developing, manufacturing and commercializing innovative neuromodulation solutions for patients with cardiovascular diseases. Barostim™ is the first medical technology approved by FDA that uses neuromodulation to improve the symptoms of patients with heart failure. Barostim is an implantable device that delivers electrical pulses to baroreceptors located in the wall of the carotid artery. The therapy is designed to restore balance to the autonomic nervous system and thereby reduce the symptoms of heart failure. Barostim received the FDA Breakthrough Device designation and is FDA-approved for use in heart failure patients in the U.S. It has been certified as compliant with the EU Medical Device Regulation (MDR) and holds CE Mark approval for heart failure and resistant hypertension in the European Economic Area. To learn more about Barostim, visit www.cvrx.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements other than statements of historical facts are forward-looking statements, including statements regarding our future financial performance (including our financial guidance regarding full year and first quarter 2026 results), our anticipated growth strategies (including statements regarding the expected timing, enrollment, scope and outcomes of the BENEFIT-HF clinical trial, potential expansion of the Barostim indication, and anticipated benefits of Barostim therapy), anticipated trends in our industry, our business prospects and our opportunities. In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “outlook,” “guidance,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential” or “continue” or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words.

The forward-looking statements in this press release are only predictions and are based largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition, and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of known and unknown risks, uncertainties and assumptions, including, but not limited to, our expectations regarding enrollment in BENEFIT-HF and the resulting impact on our addressable market; our history of significant losses, which we expect to continue; our limited history operating as a commercial company and our dependence on a single product, Barostim; our limited commercial sales experience marketing and selling Barostim; our ability to continue demonstrating to physicians and patients the merits of our Barostim; any failure by third-party payors to provide adequate coverage and reimbursement for the use of Barostim; our competitors’ success in developing and marketing products that are safer, more effective, less costly, easier to use or otherwise more attractive than Barostim; any failure to receive access to hospitals; our dependence upon third-party manufacturers and suppliers, and in some cases a limited number of suppliers; a pandemic, epidemic or outbreak of an infectious disease in the U.S. or worldwide; product liability claims; future lawsuits to protect or enforce our intellectual property, which could be expensive, time consuming and ultimately unsuccessful; any failure to retain our key executives or recruit and hire new employees; impacts on adoption and regulatory approvals resulting from additional long-term clinical data about our product; and other important factors that could cause actual results, performance or achievements to differ materially from those that are found in “Part I, Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended December 31, 2024 and “Part II, Item 1A. Risk Factors” in our Quarterly Report on Form 10-Q for the quarter ended September 30, 2025, as such factors may be updated from time to time in our other filings with the Securities and Exchange Commission. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

Investor Contact:
Mark Klausner or Mike Vallie
ICR Healthcare
443-213-0501
ir@cvrx.com

Media Contact:
Emily Meyers
CVRx, Inc.
763-416-2853
emeyers@cvrx.com

CVRx, INC.
Consolidated Balance Sheets
(In thousands, except share and per share data)
       
  December 31, December 31,
  2025
 2024
Assets      
Current assets:      
Cash and cash equivalents $75,708  $105,933 
Accounts receivable, net of allowances of $871 and $780, respectively  10,665   9,268 
Inventory  12,205   12,107 
Prepaid expenses and other current assets  3,069   2,505 
Total current assets  101,647   129,813 
Property and equipment, net  2,243   2,505 
Operating lease right-of-use asset  878   1,069 
Other non-current assets  26   27 
Total assets $104,794  $133,414 
Liabilities and Stockholders’ Equity      
Current liabilities:      
Accounts payable $3,833  $2,582 
Accrued expenses  9,484   8,180 
Total current liabilities  13,317   10,762 
Long-term debt  49,514   49,273 
Operating lease liability, non-current portion  638   877 
Other long-term liabilities  2,001   1,447 
Total liabilities  65,470   62,359 
Commitments and contingencies      
Stockholders’ equity:      
Common stock, $0.01 par value, 200,000,000 authorized as of December 31, 2025 and 2024; 26,311,607 and 25,324,684 shares issued and outstanding as of December 31, 2025 and 2024, respectively  263   253 
Additional paid-in capital  629,916   608,354 
Accumulated deficit  (590,652)   (537,346) 
Accumulated other comprehensive loss  (203)   (206) 
Total stockholders’ equity  39,324   71,055 
Total liabilities and stockholders’ equity $104,794  $133,414 


CVRx, INC.
Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share data)
             
  Three months ended Year ended
  December 31, December 31,
  2025  2024  2025  2024 
Revenue $16,024  $15,342  $56,651  $51,292 
Cost of goods sold  2,199   2,571   8,311   8,334 
Gross profit  13,825   12,771   48,340   42,958 
Operating expenses:            
Research and development  3,000   2,805   11,132   11,131 
Selling, general and administrative  22,009   20,240   88,473   91,317 
Total operating expenses  25,009   23,045   99,605   102,448 
Loss from operations  (11,184)   (10,274)   (51,265)   (59,490) 
Interest expense  (1,417)   (1,520)   (5,827)   (4,397) 
Other income, net  660   1,072   3,768   3,977 
Loss before income taxes  (11,941)   (10,722)   (53,324)   (59,910) 
Benefit (provision) for income taxes  7   71   18   (55) 
Net loss  (11,934)   (10,651)   (53,306)   (59,965) 
Cumulative translation adjustment  -   2   2   1 
Comprehensive loss $(11,934)  $(10,649)  $(53,304)  $(59,964) 
Net loss per share, basic and diluted $(0.46)  $(0.43)  $(2.04)  $(2.65) 
Weighted-average common shares used to compute net loss per share, basic and diluted  26,218,215   24,715,681   26,084,709   22,596,229 



FAQ

What were CVRx (CVRX) Q4 2025 revenue and net loss figures?

Q4 2025 revenue was $16.0 million and Q4 net loss was $11.9 million. According to the company, revenue rose 4% year-over-year while net loss widened versus Q4 2024 due to higher operating expenses and share count.

How large is the BENEFIT-HF trial CVRx announced in January 2026 (CVRX)?

The BENEFIT-HF trial will randomize 2,500 patients across about 150 centers. According to the company, it is CMS Category B IDE covered and could expand the Barostim indication up to threefold if successful.

What change occurred to CVRx's debt facility on January 9, 2026 (CVRX)?

The term loan was amended to an aggregate facility of up to $100 million, and the company borrowed an additional $10 million. According to the company, outstanding principal after borrowing is $60 million.

What 2026 financial guidance did CVRx (CVRX) provide on February 12, 2026?

CVRx guided 2026 total revenue of $63.0M–$67.0M, gross margin of 84%–86%, and operating expenses of $103M–$107M. According to the company, this reflects expected commercial momentum and trial-related investments.

How many active implanting centers did CVRx (CVRX) report at year-end 2025?

As of December 31, 2025, CVRx reported 252 active implanting centers in the U.S. According to the company, this compares to 223 centers at year-end 2024 and reflects sales territory expansion.

What are the expected BENEFIT-HF trial costs and timeline from CVRx (CVRX)?

Net trial costs are estimated at $20M–$30M spread over five to seven years, with enrollment expected to begin in Q2 2026. According to the company, the trial will evaluate Barostim in an expanded heart-failure population.
Cvrx, Inc.

NASDAQ:CVRX

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CVRX Stock Data

159.36M
23.85M
4.31%
67.77%
7.31%
Medical Devices
Surgical & Medical Instruments & Apparatus
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United States
MINNEAPOLIS