NeuroPace Receives FDA Approval for ECoG Assistant
Written by Emily J. Thompson, Senior Investment Analyst
Updated: May 29 2026
0mins
NeuroPace announced FDA approval of ECoG Assistant. This milestone represents an important step in NeuroPace's broader AI platform strategy. "This approval underscores how NeuroPace's data advantage is translating into practical tools for clinicians today," said Joel Becker, Chief Executive Officer of NeuroPace. "AI-driven insights offer the unique potential to improve the efficiency of epilepsy care now while building a platform that can unlock new opportunities over time to further personalize therapy and improve outcomes."
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Analyst Views on NPCE
Wall Street analysts forecast NPCE stock price to rise
6 Analyst Rating
6 Buy
0 Hold
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Strong Buy
Current: 16.320
Low
16.00
Averages
19.17
High
22.00
Current: 16.320
Low
16.00
Averages
19.17
High
22.00
About NPCE
NeuroPace, Inc. is a medical device company focused on transforming the lives of people living with epilepsy by reducing or eliminating the occurrence of debilitating seizures. The Company's RNS System is a brain-responsive platform that delivers personalized, real-time treatment at the seizure source. This platform can drive a better standard of care for patients living with drug-resistant epilepsy and has the potential to offer a more personalized solution and improved outcomes to the large population of patients suffering from other brain disorders. The Company's RNS System includes its RNS neurostimulator, its cortical strip leads and depth leads, and its Patient Remote Monitor, as well as other implantable and non-implantable accessories. The Company's product offerings also include Physician Tablet, Patient Data Management System (PDMS) and nSight Platform, which facilitate ongoing patient monitoring and streamline patient support. The PDMS is an online database.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
NeuroPace to Showcase New Technologies at ASSFN Meeting
- ASSFN Meeting Participation: NeuroPace will participate in the ASSFN meeting from May 29 to June 2, 2026, in Cleveland, Ohio, showcasing long-term clinical outcomes of its RNS® System, emphasizing the growing importance of responsive neuromodulation in epilepsy treatment, aimed at improving outcomes for drug-resistant epilepsy patients.
- Emerging Applications Discussion: During the meeting, NeuroPace will host a breakfast scientific symposium focused on thalamic neuromodulation, presenting NAUTILUS data in idiopathic generalized epilepsy and exploring its potential applications in broader epilepsy populations, further advancing clinical practice.
- Education and Feedback: NeuroPace will support ASSFN's educational programming focused on the fundamentals of epilepsy surgery and clinical challenges, gathering feedback from neurosurgeons on future RNS System developments to ensure the product meets clinical needs effectively.
- Technology Showcase and Support: Throughout the meeting, NeuroPace will showcase its newly FDA-approved AI tool, ECoG Assistant™, at booth #107, and conduct one-on-one meetings with clinicians to discuss clinical practice trends and the future of responsive neuromodulation, aiming to enhance patient treatment experiences and management outcomes.
See More
NeuroPace Receives FDA Approval for First AI Tool
- FDA Approval Milestone: NeuroPace announced that its first AI-driven ECoG Assistant has received FDA approval, marking a significant step in leveraging the world's only long-term intracranial EEG dataset to enhance the efficiency of epilepsy monitoring and management.
- Clinical Decision Support: The ECoG Assistant is built on 124,450 epileptologist-labeled iEEG long-episode records, enabling rapid identification of ECoGs of Interest, which supports clinicians in making faster treatment decisions and improving patient care quality.
- Future Technology Launch: NeuroPace plans to officially debut the ECoG Assistant at the American Society for Stereotactic and Functional Neurosurgery Annual Meeting on May 30, 2026, which is expected to further drive clinical adoption and enhance market competitiveness.
- Next-Generation Platform Development: The company has submitted its next-generation Patient Data Management System (PDMS) for FDA review, which, if approved, will provide a more reliable infrastructure for clinicians and patients, supporting future AI-enabled capabilities and further improving treatment outcomes.
See More
NeuroPace Reports Q1 2026 Earnings with Upgraded Revenue Guidance
- Significant Revenue Growth: NeuroPace reported total revenue of $22.1 million in Q1 2026, with $22 million excluding DIXI Medical, marking an 8% year-over-year increase, while RNS System revenue reached $21.7 million, indicating strong performance in its core business.
- Upgraded Full-Year Guidance: The company raised its full-year 2026 revenue guidance to a range of $99 million to $101 million, reflecting a growth potential of 21% to 23% in its core RNS business, excluding contributions from idiopathic generalized epilepsy, showcasing management's confidence in future growth.
- FDA Review Progress: During the quarter, the company completed its FDA mid-cycle review meeting and has responded to follow-up information requests, with management believing that a midyear determination remains on track, and expects ECoG Assistant approval in Q2 2026, further advancing its product pipeline.
- Stable Operating Expenses and Margins: The company anticipates a full-year non-GAAP gross margin between 81.5% and 82.5%, with operating expenses projected to remain in the range of $90 million to $92 million, demonstrating ongoing efforts to control costs and enhance profitability.
See More
NeuroPace Q1 Revenue Exceeds Expectations
- Revenue Performance: NeuroPace reported Q1 revenue of $22.1 million, a 1.8% year-over-year decline, yet it exceeded expectations by $0.45 million, demonstrating resilience in the market.
- Cash Flow Improvement: The company generated $8.6 million in operating cash flow during Q1, up from $7.5 million in Q1 2025, primarily due to improved operating results, although lower working capital changes impacted cash flows.
- Share Structure: As of May 5, 2026, NeuroPace had 199,696,597 issued and outstanding shares, with fully diluted shares totaling 305,626,935, indicating stability in its capital structure.
- Future Outlook: NeuroPace reiterated its revenue target of $98 million to $100 million for 2026, reflecting confidence in future growth, particularly in advancing its AI and IGE pipeline strategies.
See More
NeuroPace Releases Three-Year Study Results for RNS System
- Clinical Evidence Milestone: NeuroPace's publication of three-year results from the RNS System study shows an 82% median seizure reduction in drug-resistant focal epilepsy patients, reinforcing the system's clinical value and likely enhancing market acceptance.
- NAUTILUS Trial Progress: At the American Academy of Neurology meeting, NeuroPace presented 12- and 18-month data from the NAUTILUS trial, revealing a 77% median reduction in GTC seizures compared to baseline, indicating the system's adaptability and efficacy across a broad epilepsy patient population.
- Improved Patient Safety: The study also found a 30% decline in injury events post-treatment, with a 44% reduction in benzodiazepine use for GTC seizures compared to baseline, suggesting that the RNS System not only effectively reduces seizure frequency but also significantly enhances patients' quality of life.
- Industry Leadership Position: NeuroPace's CEO stated that the release of the three-year study results and the presentation of NAUTILUS data highlight the company's leadership in clinical evidence for neuromodulation in epilepsy, which is expected to further drive the adoption of the RNS System among drug-resistant epilepsy patients.
See More
NeuroPace to Present at 25th Annual Needham Virtual Healthcare Conference
- Presentation Schedule: NeuroPace will present at the 25th Annual Needham Virtual Healthcare Conference on April 14, 2026, at 1:30 PM ET, showcasing its latest advancements in epilepsy treatment to attract investor interest in its innovative medical devices.
- Investor Meetings: The management team will host investor meetings during the conference to facilitate interaction with potential investors, enhancing the company's market visibility and investment appeal within the medical device industry.
- Webcast Availability: The presentation will be accessible via live webcast, allowing investors to watch in real-time, and a replay will be available in the Events & Presentations section of NeuroPace's investor website for those unable to attend live, ensuring broader access to the information shared.
- Innovative Medical Device: NeuroPace's RNS System is the first commercially available brain-responsive platform designed to provide personalized, real-time treatment for drug-resistant epilepsy patients, improving their quality of life and demonstrating the company's leadership in medical technology innovation.
See More
NeuroPace to Showcase New Technologies at ASSFN Meeting
- ASSFN Meeting Participation: NeuroPace will participate in the ASSFN meeting from May 29 to June 2, 2026, in Cleveland, Ohio, showcasing long-term clinical outcomes of its RNS® System, emphasizing the growing importance of responsive neuromodulation in epilepsy treatment, aimed at improving outcomes for drug-resistant epilepsy patients.
- Emerging Applications Discussion: During the meeting, NeuroPace will host a breakfast scientific symposium focused on thalamic neuromodulation, presenting NAUTILUS data in idiopathic generalized epilepsy and exploring its potential applications in broader epilepsy populations, further advancing clinical practice.
- Education and Feedback: NeuroPace will support ASSFN's educational programming focused on the fundamentals of epilepsy surgery and clinical challenges, gathering feedback from neurosurgeons on future RNS System developments to ensure the product meets clinical needs effectively.
- Technology Showcase and Support: Throughout the meeting, NeuroPace will showcase its newly FDA-approved AI tool, ECoG Assistant™, at booth #107, and conduct one-on-one meetings with clinicians to discuss clinical practice trends and the future of responsive neuromodulation, aiming to enhance patient treatment experiences and management outcomes.
See More
NeuroPace Receives FDA Approval for First AI Tool
- FDA Approval Milestone: NeuroPace announced that its first AI-driven ECoG Assistant has received FDA approval, marking a significant step in leveraging the world's only long-term intracranial EEG dataset to enhance the efficiency of epilepsy monitoring and management.
- Clinical Decision Support: The ECoG Assistant is built on 124,450 epileptologist-labeled iEEG long-episode records, enabling rapid identification of ECoGs of Interest, which supports clinicians in making faster treatment decisions and improving patient care quality.
- Future Technology Launch: NeuroPace plans to officially debut the ECoG Assistant at the American Society for Stereotactic and Functional Neurosurgery Annual Meeting on May 30, 2026, which is expected to further drive clinical adoption and enhance market competitiveness.
- Next-Generation Platform Development: The company has submitted its next-generation Patient Data Management System (PDMS) for FDA review, which, if approved, will provide a more reliable infrastructure for clinicians and patients, supporting future AI-enabled capabilities and further improving treatment outcomes.
See More
NeuroPace Reports Q1 2026 Earnings with Upgraded Revenue Guidance
- Significant Revenue Growth: NeuroPace reported total revenue of $22.1 million in Q1 2026, with $22 million excluding DIXI Medical, marking an 8% year-over-year increase, while RNS System revenue reached $21.7 million, indicating strong performance in its core business.
- Upgraded Full-Year Guidance: The company raised its full-year 2026 revenue guidance to a range of $99 million to $101 million, reflecting a growth potential of 21% to 23% in its core RNS business, excluding contributions from idiopathic generalized epilepsy, showcasing management's confidence in future growth.
- FDA Review Progress: During the quarter, the company completed its FDA mid-cycle review meeting and has responded to follow-up information requests, with management believing that a midyear determination remains on track, and expects ECoG Assistant approval in Q2 2026, further advancing its product pipeline.
- Stable Operating Expenses and Margins: The company anticipates a full-year non-GAAP gross margin between 81.5% and 82.5%, with operating expenses projected to remain in the range of $90 million to $92 million, demonstrating ongoing efforts to control costs and enhance profitability.
See More
NeuroPace Q1 Revenue Exceeds Expectations
- Revenue Performance: NeuroPace reported Q1 revenue of $22.1 million, a 1.8% year-over-year decline, yet it exceeded expectations by $0.45 million, demonstrating resilience in the market.
- Cash Flow Improvement: The company generated $8.6 million in operating cash flow during Q1, up from $7.5 million in Q1 2025, primarily due to improved operating results, although lower working capital changes impacted cash flows.
- Share Structure: As of May 5, 2026, NeuroPace had 199,696,597 issued and outstanding shares, with fully diluted shares totaling 305,626,935, indicating stability in its capital structure.
- Future Outlook: NeuroPace reiterated its revenue target of $98 million to $100 million for 2026, reflecting confidence in future growth, particularly in advancing its AI and IGE pipeline strategies.
See More
NeuroPace Releases Three-Year Study Results for RNS System
- Clinical Evidence Milestone: NeuroPace's publication of three-year results from the RNS System study shows an 82% median seizure reduction in drug-resistant focal epilepsy patients, reinforcing the system's clinical value and likely enhancing market acceptance.
- NAUTILUS Trial Progress: At the American Academy of Neurology meeting, NeuroPace presented 12- and 18-month data from the NAUTILUS trial, revealing a 77% median reduction in GTC seizures compared to baseline, indicating the system's adaptability and efficacy across a broad epilepsy patient population.
- Improved Patient Safety: The study also found a 30% decline in injury events post-treatment, with a 44% reduction in benzodiazepine use for GTC seizures compared to baseline, suggesting that the RNS System not only effectively reduces seizure frequency but also significantly enhances patients' quality of life.
- Industry Leadership Position: NeuroPace's CEO stated that the release of the three-year study results and the presentation of NAUTILUS data highlight the company's leadership in clinical evidence for neuromodulation in epilepsy, which is expected to further drive the adoption of the RNS System among drug-resistant epilepsy patients.
See More
NeuroPace to Present at 25th Annual Needham Virtual Healthcare Conference
- Presentation Schedule: NeuroPace will present at the 25th Annual Needham Virtual Healthcare Conference on April 14, 2026, at 1:30 PM ET, showcasing its latest advancements in epilepsy treatment to attract investor interest in its innovative medical devices.
- Investor Meetings: The management team will host investor meetings during the conference to facilitate interaction with potential investors, enhancing the company's market visibility and investment appeal within the medical device industry.
- Webcast Availability: The presentation will be accessible via live webcast, allowing investors to watch in real-time, and a replay will be available in the Events & Presentations section of NeuroPace's investor website for those unable to attend live, ensuring broader access to the information shared.
- Innovative Medical Device: NeuroPace's RNS System is the first commercially available brain-responsive platform designed to provide personalized, real-time treatment for drug-resistant epilepsy patients, improving their quality of life and demonstrating the company's leadership in medical technology innovation.
See More
