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NeurAxis Reports Record Second Quarter 2026 Financial Results Driven by 116% Year Over Year Revenue Growth

(Moderate)
(Very Positive)
Tags

NeurAxis (NYSE American: NRXS) reported record second quarter 2026 results, with revenues rising 116% year over year to $1.93 million, driven by increased payer coverage following the January 1, 2026 Category I CPT code for Percutaneous Electrical Nerve Field Stimulation (PENFS).

Unit deliveries grew 60% year over year and gross margin improved to 85.9% from 83.6%, reflecting a shift from discounted assistance programs to fully reimbursed procedures. Cash stood at $8.3 million on June 30, 2026, with operating cash use reduced to $1.0 million versus $1.5 million a year earlier.

The company highlighted several milestones: VA Federal Supply Schedule contract award, first-ever FDA clearance for IB-Stim in functional dyspepsia abdominal pain (ages 8+), and pediatric guidelines recommending its PENFS technology for functional abdominal pain in IBS.

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Positive

  • Revenue +116% YoY to $1.93M in Q2 2026
  • Unit deliveries +60% YoY in Q2 2026
  • Gross margin improved to 85.9% from 83.6% year over year
  • Cash balance of $8.3M as of June 30, 2026
  • Operating cash use reduced to $1.0M from $1.5M year over year
  • First FDA clearance for IB-Stim in functional dyspepsia abdominal pain
  • Awarded VA Federal Supply Schedule contract, opening access to VA system
  • Category I CPT code effective for PENFS, supporting broader payer coverage

Negative

  • Q2 2026 net loss of $2.09M vs $1.69M in Q2 2025
  • Operating loss of $2.12M vs $1.72M in Q2 2025
  • Selling expenses increased to $0.86M from $0.53M year over year
  • R&D expenses rose to $0.27M from $0.12M year over year
  • G&A expenses grew to $2.65M from $1.82M year over year

News Explained

The $2.5 million liquidity improvement includes ATM activity, but its share count and dilution effect remain unquantified.

NeurAxis reports a $2.5 million liquidity improvement from its at-the-market facility, warrant redemptions and lower operating cash outflows; the ATM portion involves selling newly issued shares, which can reduce existing holders’ ownership percentage.

An ATM program lets the issuer sell new shares gradually at prevailing market prices rather than through one single priced deal. The release does not say how much of the $2.5 million came from the ATM or how many shares were sold, so the ownership effect cannot be quantified from this disclosure.

The August 11, 2026 10-Q is the specific filing whose equity-issuance and cash-flow line items can resolve that breakdown.

Sources and calculations

Market Reaction – NRXS

+1.89% $7.00 2.7x vol
15m delay
+1.89% Vs previous close
$7.00 Last Price
$6.53 $7.30 Day Range
$90.14M Market Cap
2.7x Rel. Volume

Following this news, NRXS has gained 1.89%, reflecting a mild positive market reaction. The stock is currently trading at $7.00. Trading volume is elevated at 2.7x the average, suggesting notable buying interest.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Gold for real-time data.

Market Context

NRXS had a low short-positioning signal in the provided risk context. The quarter’s revenue growth a...
Analysis

NRXS had a low short-positioning signal in the provided risk context. The quarter’s revenue growth and higher margin can be weighed against continuing losses; the active S-3/A is a resale registration, not company financing.

Key Figures

Revenue: $1.9M, up 116% YoY Gross Margin: 85.9% Cash Balance: $8.3M +5 more
8 metrics
Revenue $1.9M, up 116% YoY 2Q26 versus 2Q25
Gross Margin 85.9% 2Q26 versus 83.6% in 2Q25
Cash Balance $8.3M As of June 30, 2026
Cash Used in Operations $1.0M 2Q26 versus $1.5M in 2Q25
Unit Deliveries Up 60% YoY 2Q26
FDA Clearance Patients 8 years and older Functional dyspepsia with associated nausea symptoms
Net Loss $2,085,746 2Q26 versus $1,690,418 in 2Q25
Liquidity Raised $2.5M ATM facility, warrant redemptions, and lower operating cash outflows

Previous Earnings Reports

5 past events · Latest: May 12 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 12 1Q26 earnings Positive +1.5% Revenue growth, margin expansion, and improved operating loss supported quarterly results.
Mar 19 4Q25 earnings Positive +2.4% Quarterly and full-year revenue growth accompanied strategic commercial milestones.
Nov 11 3Q25 earnings Positive -5.9% Revenue increased, but margin pressure and wider operating loss accompanied reported milestones.
Aug 12 2Q25 earnings Positive +2.5% Revenue growth, improved operating loss, and expanded clinical milestones marked the quarter.
May 12 1Q25 earnings Positive +16.0% Revenue growth and expanded covered lives accompanied product and regulatory milestones.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Tag-specific earnings reactions were positive in four of five prior events, with one negative divergence despite positive reported results.

Key Terms

category i cpt code, at-the-market facility, functional dyspepsia, neuromodulation
4 terms
category i cpt code regulatory
"Category I CPT code assignment for Percutaneous Electric 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.
at-the-market facility financial
"raising $2.5 million through its at-the-market facility"
An at-the-market facility is a standing arrangement that lets a publicly traded company sell new shares directly into the open market at whatever the current market price is, typically through an investment bank acting as a sales agent. For investors it matters because it provides the company with a flexible way to raise cash without a large, one-time share offering; however, selling additional shares can dilute existing ownership and, by increasing supply, may pressure the stock price like adding more tickets to a limited-seat event.
functional dyspepsia medical
"FDA clearance for the treatment of abdominal pain in functional dyspepsia"
A common chronic disorder of the upper digestive tract that causes recurring stomach discomfort, bloating, early fullness, and nausea without an obvious structural cause. Think of it as a repeatedly upset stomach that persists and interferes with daily life; for investors it matters because its high prevalence and limited effective treatments drive demand for new drugs, diagnostics, and therapies, affecting commercial prospects and regulatory attention in the gastrointestinal market.
neuromodulation medical
"a medical technology company commercializing neuromodulation therapies"
Neuromodulation is the use of devices or targeted treatments to change how nerves or brain circuits send signals, much like adjusting the volume or tuning on an audio system to alter what you hear. For investors, it matters because these therapies can treat chronic conditions (pain, movement disorders, depression) where existing medicines fall short, creating potential markets, regulatory milestones, and durable revenue streams if technologies prove safe and effective.

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

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Conference call will be held today, Tuesday, August 11 at 9:00 am ET

CARMEL, Ind., Aug. 11, 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 second quarter period ended June 30, 2026.

2Q26 Financial Highlights

  • Revenues increased 116% year over year to $1.9M, reflecting continued growth from the Category I CPT code assignment for Percutaneous Electric Nerve Field Stimulation (PENFS) effective January 1, 2026, substantially increasing payer coverage.
  • Expanded gross margin by 230 basis points as significantly more devices were sold at full reimbursement price reflective of the Category I CPT code payer coverage.
  • Cash balance of $8.3 million as of June 30, 2026. Cash used in operations of $1.0 million in the second quarter of 2026 vs. $1.5 million in the second quarter of 2025.

Recent Operational Highlights

  • Category I CPT® code assignment to report Percutaneous Electrical Nerve Field Stimulation (PENFS) procedures is now effective, 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, demonstrating a clear commercial pathway into the Veterans Affairs health system, which serves ~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 important 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.

Management Commentary

Brian Carrico, Chief Executive Officer of NeurAxis, commented: "Our second quarter results exceeded our expectations, but more importantly, we applied the insights gained during the first quarter to make meaningful strategic adjustments and additions that further strengthen our commercial execution. The second quarter again confirmed both the strength of demand for PENFS nationally and the effectiveness of our commercial model. It also reinforced that utilization is highest in markets where access barriers are lower and providers have the right combination of payer coverage, physician engagement, and operational capacity. As a result, we have expanded our commercial organization to focus on regions where insurance coverage is strongest, positioning us to maximize adoption and growth.

"During the quarter, we also continued to improve our average selling price as our revenue mix shifted toward covered and reimbursed procedures and away from discounted financial assistance programs. This transition enhances the quality of our revenue, supports stronger long-term gross margins, and provides a more scalable foundation for future growth. In addition, market feedback continues to reinforce that PENFS is among the most profitable pediatric gastroenterology procedures performed in the office setting when supported by commercial insurance coverage.

"Expanding insurance coverage remains the single most important driver of our long-term growth strategy. While the progress we have made with commercial payers has been encouraging, our experience continues to demonstrate that providers require confidence that a meaningful portion of their patient population is covered before they fully integrate PENFS into routine clinical practice. Accordingly, expanding medical policy coverage remains our highest strategic priority.

"We continue to make meaningful progress with several large commercial payers and are cautiously optimistic that these efforts will result in additional coverage decisions during the second half of 2026 or early 2027. At the same time, we are applying these proven strategies across our broader payer pipeline while enhancing the operational infrastructure that enables providers to efficiently treat patients once coverage is established.

"With a growing base of commercial insurance coverage, increasing physician adoption, and an increasingly focused commercial organization, we believe NeurAxis has successfully transitioned from an access-creation phase to an execution phase. We remain confident that our commercial strategy, combined with continued payer expansion, positions the Company to drive sustainable long-term growth."

Second Quarter 2026 Financial Results

Revenues in the second quarter of 2026 were $1.9 million, up 116% compared to 894 thousand in the second quarter of 2025. Unit deliveries increased 60% year over year due to the Category I CPT code for PENFS becoming effective January 1, 2026, and the corresponding increased payer coverage.

Gross margin in the second quarter of 2026 increased to 85.9% from 83.6% in the second quarter of 2025 due to a mix shift in unit deliveries from patients utilizing the Company’s discounted financial assistance program to full reimbursement payers on account of the Category I CPT code.

Selling expenses were $861 thousand in the second quarter of 2026 compared to $534 thousand in the second quarter of 2025 driven by the Company’s strong sales growth.

Research and development expenses in the second quarter of 2026 of were $274 thousand compared to $116 thousand in the second quarter of 2025 as the Company launched more clinical research studies to advance its adult indications and pursue further IB-Stim indications.

General and administrative expenses were $2.6 million for the second quarter of 2026, compared to $1.8 million for the second quarter of 2025. The increase was primarily attributable to increased sales, marketing and market access headcount and related advisory services to support the Company’s growth, incremental stock compensation expense associated with the third year of a three-year equity award plan and higher incentive compensation driven by improved operating performance.

Operating loss and net loss in the second quarter of 2026 increased 24% and 23%, respectively, compared to the first quarter of 2025.

Cash on hand as of June 30, 2026, was $8.3 million. The Company improved its liquidity position in the second quarter of 2026 by raising $2.5 million through its at-the-market facility, warrant redemptions and lower operating cash outflows.

Conference Call Details

Date and Time: Tuesday, August 11, 2026, at 9:00am ET

Toll Free: 1-877-270-2148 (U.S. and Canada toll-free) International: 1-412-317-6060
Webcast: https://app.webinar.net/E5zrP9X7wLY

Replay: Toll Free: 1-855-669-9658 (U.S. and Canada toll-free) International: 1-412-317-0088

Replay access code: 8443629

Webcast: https://app.webinar.net/E5zrP9X7wLY

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
(Unaudited)
    
 Three Months Ended June 30, Six Months Ended June 30,
  2026   2025   2026   2025 
        
Net sales$1,928,695  $894,086  $3,536,578  $1,789,741 
Cost of goods sold 272,573   146,643   490,939   286,118 
Gross profit 1,656,122   747,443   3,045,639   1,503,623 
Selling expenses 861,387   534,013   1,685,724   1,034,131 
Research and development 274,344   115,197   373,911   222,201 
General and administrative 2,645,103   1,816,091   4,851,395   4,260,246 
Operating loss (2,124,712)  (1,717,858)  (3,865,391)  (4,012,955)
Other income (expense):       
Interest expense, net (19,794)  (13,434)  (45,983)  (15,672)
Change in fair value of warrant liability 2,449   (119)  (29,057)  1,712 
Other income 56,311   40,993   93,253   57,813 
Total other income, net 38,966   27,440   18,213   43,853 
Loss before income taxes (2,085,746)  (1,690,418)  (3,847,178)  (3,969,102)
Income tax expense -   -   -   - 
Net loss$ (2,085,746) $ (1,690,418) $ (3,847,178) $ (3,969,102)



FAQ

How did NeurAxis (NRXS) perform financially in Q2 2026?

NeurAxis reported Q2 2026 revenue of $1.93 million, up 116% year over year. According to NeurAxis, unit deliveries rose 60%, and gross margin improved to 85.9% as more procedures were reimbursed at full price under the new Category I CPT code.

What drove NeurAxis (NRXS) revenue growth of 116% year over year in Q2 2026?

Revenue growth to $1.93 million was mainly driven by the Category I CPT code for PENFS effective January 1, 2026. According to NeurAxis, this substantially increased payer coverage and shifted volumes from discounted assistance programs to fully reimbursed procedures.

Did NeurAxis (NRXS) remain profitable in the second quarter of 2026?

NeurAxis remained unprofitable, reporting a Q2 2026 net loss of $2.09 million. According to NeurAxis, higher selling, research and development, and general and administrative expenses outweighed gross profit gains, although operating cash usage improved from the prior-year quarter.

What is NeurAxis’s cash position and liquidity as of June 30, 2026?

NeurAxis reported cash of $8.3 million as of June 30, 2026. According to NeurAxis, liquidity improved through $2.5 million raised via an at-the-market facility and warrant redemptions, combined with lower operating cash outflows of $1.0 million in the quarter.

What new regulatory and clinical milestones did NeurAxis (NRXS) achieve in 2026?

NeurAxis obtained the first FDA clearance for treating abdominal pain in functional dyspepsia with IB-Stim in patients 8 and older. According to NeurAxis, its PENFS technology was also recommended in pediatric guidelines for functional abdominal pain in IBS, supporting broader adoption.

How does the VA Federal Supply Schedule contract impact NeurAxis (NRXS)?

The VA Federal Supply Schedule contract designates NeurAxis as a federal contractor and provides a commercial pathway into the Veterans Affairs health system. According to NeurAxis, the VA system serves about 7 million patients annually, representing a significant access opportunity for IB-Stim.

When did NeurAxis (NRXS) hold its Q2 2026 earnings conference call?

NeurAxis held its Q2 2026 earnings conference call on Tuesday, August 11, 2026, at 9:00 a.m. ET. According to NeurAxis, the call was accessible via toll-free and international dial-in numbers and a webcast link with a recorded replay option.