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NeurAxis Reports Strong Fourth Quarter and Full Year 2025 Financial Results

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NeurAxis (NYSE: NRXS) reported strong revenue growth and strategic commercial wins for 4Q25 and FY2025. Revenue grew 27% in 4Q25 to $968k and 33% for FY2025 to $3.6M. Operating loss widened to $1.7M in 4Q25 and $7.8M for FY2025; cash was $5.0M at year-end.

Key commercial milestones include a Category I CPT code effective Jan 1, 2026, a VA Federal Supply Schedule contract, expanded FDA clearance for IB-Stim for abdominal pain in patients 8+ years, and post-year At-The-Market proceeds of $2.6M.

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Positive

  • Revenue +33% FY2025 to $3.6M
  • Unit sales +44% FY2025
  • Category I CPT code effective Jan 1, 2026; >100M covered lives
  • VA Federal Supply Schedule contract awarded
  • FDA clearance expanded to treat abdominal pain in patients 8 years+
  • Raised $2.6M post-year via ATM and warrants

Negative

  • Operating loss +9% FY2025 to $7.8M
  • Operating loss +17% Q4 2025 to $1.7M
  • Cash used in operations $6.4M in FY2025
  • Year-end cash $5.0M may pressure short-term liquidity
  • SG&A expenses +14% FY2025 driven by legal settlement and hiring

Key Figures

Q4 2025 revenue: $968,000 FY2025 revenue: $3.6 million Q4 2025 gross margin: 85.4% +5 more
8 metrics
Q4 2025 revenue $968,000 Fourth quarter 2025; 27% year-over-year increase vs Q4 2024
FY2025 revenue $3.6 million Full year 2025; 33% year-over-year increase vs FY2024
Q4 2025 gross margin 85.4% Fourth quarter 2025; down 100 bps from 86.4% in Q4 2024
FY2025 gross margin 84.2% Full year 2025; down 130 bps from 86.5% in FY2024
FY2025 operating loss $7.8 million Full year 2025; 9% increase vs $7.2 million in FY2024
Q4 2025 operating loss $1.7 million Fourth quarter 2025; 17% increase vs $1.5 million in Q4 2024
Cash balance $5.0 million Cash on hand as of December 31, 2025
ATM and warrants proceeds $2.6 million Raised subsequent to year-end via At-The-Market offering and warrant exercises

Market Reality Check

Price: $6.99 Vol: Volume 395,160 is 2.03x t...
high vol
$6.99 Last Close
Volume Volume 395,160 is 2.03x the 20-day average of 194,428, showing elevated trading activity before this release. high
Technical Shares at $6.99 are trading above the 200-day MA of $3.37 and sit 6.3% below the 52-week high.

Peers on Argus

NRXS fell 3.05% while key peers AKTX (-18.21%), ICU (-4.08%), LIXT (-4.41%), and...

NRXS fell 3.05% while key peers AKTX (-18.21%), ICU (-4.08%), LIXT (-4.41%), and RNTX (-4.96%) also traded lower, but no peers appeared in the momentum scanner, pointing to a stock-specific move rather than a coordinated sector rotation.

Previous Earnings Reports

5 past events · Latest: Mar 12 (Neutral)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 12 Earnings call notice Neutral +0.5% Scheduled Q4 and FY2025 results call with webcast and Q&A details.
Nov 11 Q3 2025 results Positive -5.9% Q3 2025 revenue up 22% with higher unit growth but wider operating loss.
Aug 12 Q2 2025 results Positive +2.5% Q2 2025 revenue growth of 46% and improved operating loss with strong milestones.
May 12 Q1 2025 results Positive +16.0% Q1 2025 revenue up 39% and expanded coverage to 51 million lives.
Mar 20 Q4 2024 results Positive -0.9% Q4 2024 revenue up 43% and FY2024 revenue of $2.7M with better losses.
Pattern Detected

Earnings and related updates have generally been received positively, but there are notable instances where strong growth headlines coincided with negative next-day moves.

Recent Company History

Across prior earnings-linked events, NeurAxis repeatedly highlighted strong year-over-year revenue growth, such as Q1 2025 revenue rising to $896,000, Q2 to $894,000, Q3 to $811,000, and FY2024 revenue of $2.7 million. These were paired with expanding covered lives (up to 55 million) and reimbursement milestones like the Category I CPT code effective January 1, 2026. However, price reactions have been mixed, with some strong reports (e.g., Q1 2025, +16%) followed by others where good fundamentals were met with selling.

Historical Comparison

+2.4% avg move · Past earnings and related updates for NRXS moved the stock an average of 2.44% over 24 hours. Today’...
earnings
+2.4%
Average Historical Move earnings

Past earnings and related updates for NRXS moved the stock an average of 2.44% over 24 hours. Today’s -3.05% reaction to strong FY2025 growth sits on the weaker side of that history.

Earnings updates across Q1–Q3 2025 showed revenue growth of 39%, 46%, and 22%, followed by FY2024 revenue of $2.7M and now FY2025 revenue of $3.6M, reflecting a consistent expansion trajectory alongside reimbursement and coverage milestones.

Market Pulse Summary

This announcement details strong Q4 and FY2025 revenue growth—up 27% and 33% year over year—alongsid...
Analysis

This announcement details strong Q4 and FY2025 revenue growth—up 27% and 33% year over year—alongside high gross margins in the mid-80% range but larger operating losses of $1.7 million for Q4 and $7.8 million for the year. Key milestones include a Category I CPT code, VA FSS contract, and expanded FDA clearances for IB-Stim. Investors may watch cash use, now $5.0 million year-end plus $2.6 million raised post‑period, and how reimbursement and unit growth balance margin pressure.

Key Terms

category i cpt code, fda clearance, at-the-market equity offering, cpt code
4 terms
category i cpt code regulatory
"Category I CPT® code assignment to report Percutaneous Electrical Nerve Field Stimulation"
A Category I CPT code is a five-digit medical billing number used to describe commonly performed procedures and services so insurers and providers speak the same language when submitting claims and paying bills. For investors, these codes matter because they determine how easily and consistently a treatment or test can be billed and reimbursed—think of them like a standardized barcode that helps forecast revenue, adoption, and insurance coverage risks for healthcare products and services.
fda clearance regulatory
"Awarded the first-ever FDA clearance for the treatment of abdominal pain in functional dyspepsia"
FDA clearance is the U.S. Food and Drug Administration’s official permission to market certain medical devices or diagnostic tests after reviewing evidence that they are as safe and effective as similar products already on the market. For investors, it’s like a product passing a required safety inspection — it reduces regulatory uncertainty, speeds commercial rollout, and can directly affect sales prospects, valuation, and partnership opportunities.
at-the-market equity offering financial
"the Company secured an additional $2.6 million through its At-The-Market equity offering and warrant"
An at-the-market equity offering is a way for a public company to raise cash by selling newly issued shares directly into the open market at current market prices over time through a broker. Think of it as gradually selling items on an online marketplace at whatever buyers are paying now rather than holding a single big sale; it gives the company flexible access to funds but can lower each existing owner’s share of the company and put gentle downward pressure on the stock price if done in large amounts.
cpt code regulatory
"transitioned from a Category III CPT code to a Category I CPT code effective January 1, 2026"
A CPT code is a standardized numeric label used by healthcare providers and insurers to identify medical procedures, tests, and services for billing and reimbursement. Think of it as a SKU or price tag for each clinical service: which code is used and how it’s reimbursed directly affects a provider’s revenue and a medical product’s market adoption, so investors watch codes and payment rules to estimate financial impact.

AI-generated analysis. Not financial advice.

Conference call will be held today, Thursday, March 19 at 9:00 am ET

CARMEL, Ind., March 19, 2026 (GLOBE NEWSWIRE) -- NeurAxis, Inc. (“NeurAxis,” or the “Company”) (NYSE American: NRXS), a medical technology company commercializing neuromodulation therapies for chronic and debilitating conditions in children and adults, today announced results for the fourth quarter period and full year ended December 31, 2025.

4Q25 Financial Highlights

  • Revenues increased 27% year over year to $968 thousand in 4Q25.
  • Operating loss increased 17% year over year, primarily due to higher selling expenses directly related to increased sales volume and compensation expenses to facilitate growth.  
  • Cash balance was $5.0 million as of December 31, 2025.

FY2025 Financial Highlights

  • Revenues for FY2025 increased 33% year over year to $3.6 million.
  • Operating loss increased 9% year over year, primarily due to a one-time non-recurring legal settlement. Excluding the legal settlement, the Company’s operating loss was flat year over year despite its investment in selling expenses that were offset by higher gross profit from increased sales volume.

Recent Operational Highlights

  • Category I CPT® code assignment to report Percutaneous Electrical Nerve Field Stimulation (PENFS) procedures is now in effect, completing a successful commercial milestone for the Company’s proprietary technology, IB-Stim®.
  • Awarded a Veterans Affairs Federal Supply Schedule (FSS) contract, officially designating NeurAxis as a federal contractor and creates a clear commercial pathway into the Veterans Affairs health system, which serves nearly 7 million patients annually. 
  • Awarded the first-ever FDA clearance for the treatment of abdominal pain in functional dyspepsia (FD), with associated nausea symptoms, in patients 8 years of age and older, expanding the total addressable market for IB-Stim.
  • Secured key academic society guidelines recommendation for treatment of functional abdominal pain (FAP) in irritable bowel syndrome (IBS) in pediatrics. NeurAxis’s PENFS technology is the only FDA-cleared or approved treatment recommended in the pediatrics guidelines, enabling momentum for large-scale insurance coverage for IB-Stim.
  • Received and expanded FDA clearance for the age and treatment time per patient for IB-Stim:
    • The age range expanded from 8-21 years to 8 years and older.
    • The recommended treatment per patient increased from 3 devices to 4 devices, one device per week, for 4 consecutive weeks.

Management Commentary

Brian Carrico, Chief Executive Officer of NeurAxis, commented: “We believe NeurAxis has entered a new phase of its growth trajectory. With the Category I CPT code now in effect with positive policy coverage for more than 100 million covered lives, the foundation for scalable adoption of IB-Stim is firmly in place, and the opportunity in front of us is significantly easier for the market to understand.

Our highest priority remains expanding medical policy coverage across the payer landscape, as each additional coverage win meaningfully increases patient access and reduces friction for providers. In parallel, our internal prior-authorization team continues to expand, helping hospital partners streamline reimbursement and increase confidence in adopting IB-Stim.

The early part of 2026 has been focused on deploying our commercial strategy, learning from real-world utilization, and identifying the key drivers that accelerate adoption. With those insights now in hand and the reimbursement framework established, we believe we are positioned at the beginning of a multi-year growth cycle, with our focus squarely on disciplined execution and scaling utilization nationwide.”

Fourth Quarter and Fiscal Year 2025 Financial Results

Revenues in the fourth quarter of 2025 were $968 thousand, up 27% compared to $761 thousand in the fourth quarter of 2024. Unit sales increased approximately 35% due to growth from patients with full insurance reimbursement and the Company’s launch of the RED device in 2025, a screening tool for chronic constipation. The fourth quarter of 2025 marked a shift in mix from discounted financial assistance to full reimbursement sales as the Company transitioned from a Category III CPT code to a Category I CPT code effective January 1, 2026.

Revenue in fiscal year 2025 was $3.6 million, an increase of 33% compared to $2.7 million in fiscal year 2024. Unit sales increased approximately 44% with growth from the financial assistance programs outpacing that of patients with full insurance coverage, supplemented by new RED device sales.

Gross margin in the fourth quarter of 2025 of 85.4% declined 100 basis points compared to 86.4% in the fourth quarter of 2024 due to higher discounting in the financial assistance program to patients with lower income levels and the lower margin profile of the RED device.

Gross margin in fiscal year 2025 of 84.2% declined 130 basis points compared to 86.5% in fiscal year 2024 due to higher growth from and discounting of the Company's financial assistance programs and charges related to expired RED inventory.

Selling, general and administrative expenses in the fourth quarter of 2025 were $2.5 million, an increase of 20% compared to $2.1 million in the fourth quarter of 2024. The increase was due to higher commission directly attributable to higher sales volume quarter over quarter and stock compensation costs associated with the introduction of a long-term incentive plan in 2025, which did not exist in 2024.

Selling, general, and administrative expenses in fiscal year 2025 were $10.8 million, an increase of 14% compared to $9.5 million in fiscal year 2024. The increase was due to a one-time, non-recurring legal settlement, hiring of key sales and marketing personnel, incremental marketing costs focused on health insurance carriers, and the introduction of a long-term incentive plan in 2025, which did not exist in 2024.

Operating loss in the fourth quarter of 2025 was $1.7 million, an increase of 17% compared to $1.5 million in the fourth quarter of 2024.

Operating loss in fiscal year 2025 was $7.8 million, an increase of 9% compared to the $7.2 million for the full year of 2024.

Net loss in the fourth quarter of 2025 was $1.7 million, an increase of 18% compared to $1.4 million in the fourth quarter of 2024, primarily due to the higher operating loss.

Net loss for the full year 2025 was $7.8 million, a decrease of 5% compared to $8.2 million for the full year of 2024, primarily due to the absence of one-time, non-recurring 2024 settlements related to a convertible note dispute and certain pre-IPO Series A Preferred Stock shareholder claims, partially offset by the higher operating loss.  

Cash on hand as of December 31, 2025, was $5.0 million. As of December 31, 2025, the Company had $148 thousand and $10 thousand of short-term and long-term debt, respectively. Cash used in operations in fiscal year 2025 of $6.4 million was $335 thousand higher than in fiscal year 2024 primarily due to the payment of the 2024 short-term incentive program in 2025 and higher inventory purchases as the Company prepared for the transition of its IB-Stim device from a Category III CPT code to a Category I CPT code effective January 1, 2026, partially offset by better receivable collections. Subsequent to year end, the Company secured an additional $2.6 million through its At-The-Market equity offering and warrant exercises.

Conference Call Details

Date and Time: Thursday, March 19, 2026, at 9:00am ET

Live Webcast Information: Interested parties can access the conference call via a live webcast, which is available in the Investor Relations section of the Company's website at https://ir.neuraxis.com/ or https://edge.media-server.com/mmc/p/4ig827me. For participants listening through the webcast, questions can be sent in through the portal using the “Ask a Question” link or by emailing questions to NRXS@lythampartners.com.

Call-in Information: Interested parties can also access the live conference call by initially registering at the following link. Upon completion of the registration link, call-in participants will receive the dial-in info and a unique PIN to join the call as well as an email confirmation with the details.

Replay: A webcast replay will be available in the Investor Relations section of the Company's website at https://ir.neuraxis.com/ or https://edge.media-server.com/mmc/p/4ig827me.

About NeurAxis, Inc.

NeurAxis, Inc., is a medical technology company focused on neuromodulation therapies to address chronic and debilitating conditions in children and adults. NeurAxis is dedicated to advancing science and leveraging evidence-based medicine to drive the adoption of IB-Stim, its proprietary Percutaneous Electrical Nerve Field Stimulation (PENFS) technology, by the medical, scientific, and patient communities. IB-Stim is FDA-cleared for functional abdominal pain in irritable bowel syndrome (IBS) and functional dyspepsia, including FD-linked nausea symptoms in patients ages 8 and older. Additional clinical trials of PENFS in multiple pediatric and adult conditions with large unmet healthcare needs are underway. For more information, please visit http://neuraxis.com.

Forward-Looking Statements

Certain statements in this press release are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements other than statements of historical fact are forward-looking statements. Forward-looking statements are based on management’s current assumptions and expectations of future events and trends, which affect or may affect the Company’s business, strategy, operations or financial performance, and actual results and other events may differ materially from those expressed or implied in such statements due to numerous risks and uncertainties. Forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified. There are a number of important factors that could cause actual results, developments, business decisions or other events to differ materially from those contemplated by the forward-looking statements in this press release. These factors include, among other things, the conditions in the U.S. and global economy, the trading price and volatility of the Company’s stock, public health issues or other events, the Company’s compliance with applicable laws, the results of the Company’s clinical trials and perceptions thereof, the results of submissions to the FDA, and factors described in the Risk Factors section of NeurAxis’s public filings with the Securities and Exchange Commission (SEC). Because forward-looking statements are inherently subject to risks and uncertainties, you should not rely on these forward-looking statements as predictions of future events. These forward-looking statements speak only as of the date of this press release and, except to the extent required by applicable law, the Company undertakes no obligation to update or revise these statements, whether as a result of any new information, future events and developments or otherwise.

For contraindications, precautions, warnings, and IFU, please see: https://ibstim.com/important-information/.

For important RED information, including indications, precautions, and contraindications, visit: https://red4constipation.com/information/

Contacts:

Company
NeurAxis, Inc.
info@neuraxis.com

Investor Relations
Lytham Partners
Ben Shamsian
646-829-9701
shamsian@lythampartners.com

 
NeurAxis, Inc.
Condensed Statements of Operations
  
 For the Years Ended December 31,
 2025
 2024
    
Net sales$3,569,282  $2,685,925 
Cost of goods sold 562,916   362,002 
Gross profit 3,006,366   2,323,923 
Selling expenses 2,279,974   1,468,884 
Research and development 493,611   433,614 
General and administrative 8,062,689   7,578,242 
Operating loss (7,829,908)  (7,156,817)
Other income (expense):   
Financing charges (30,240)  (230,824)
Interest expense, net (73,969)  (174,328)
Change in fair value of warrant liability (7,634)  (941)
Amortization of debt discount and issuance costs -   (126,387)
Other income (expense) 141,196   (552,204)
Total other income (expense), net 29,353   (1,084,684)
Net loss$ (7,800,555) $ (8,241,501)



FAQ

What were NeurAxis (NRXS) revenue and growth for Q4 2025 and FY2025?

NeurAxis reported $968k revenue in Q4 2025 and $3.6M for FY2025. According to the company, Q4 revenue rose 27% year-over-year and full-year revenue increased 33%, driven by higher unit sales and RED device launches.

How did NeurAxis (NRXS) profitability and losses change in FY2025?

Operating loss increased to $7.8M in FY2025, up 9% year-over-year. According to the company, the rise reflected a one-time legal settlement, higher selling costs for growth, and investments in sales and marketing.

What commercial milestones did NeurAxis (NRXS) announce on March 19, 2026?

NeurAxis secured a Category I CPT code and a VA Federal Supply Schedule contract. According to the company, these milestones broaden reimbursement pathways and create a clearer commercial route into VA systems serving nearly 7 million patients annually.

What FDA and clinical expansions did NeurAxis (NRXS) report for IB-Stim?

The FDA clearance now includes treatment of abdominal pain in functional dyspepsia for patients aged 8 years and older. According to the company, treatment recommendations increased to four devices per patient, expanding the addressable pediatric market.

What is NeurAxis's cash position and recent financing as of March 19, 2026?

NeurAxis had $5.0M cash at December 31, 2025 and secured $2.6M post-year via ATM and warrant exercises. According to the company, the financings supplemented year-end liquidity amid operational cash use.
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75.10M
8.18M
Biotechnology
Electromedical & Electrotherapeutic Apparatus
Link
United States
CARMEL