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26.07.2021 19:54:00

Evren Technologies receives FDA Breakthrough Device Designation for the Phoenix® - Revolutionary Transcutaneous Auricular Vagus Nerve Therapy to Treat PTSD

GAINESVILLE, Fla., July 26, 2021 /PRNewswire/ -- Evren Technologies, Inc. announced today that its non-invasive Phoenix® earbud device received Breakthrough Device Designation from the U.S. Food and Drug Administration for the treatment of Post-traumatic Stress Disorder (PTSD).

Evren Technologies is advancing the treatment of PTSD through a user-friendly and intelligent platform that is easy to use and personalized. Our initial medical device - the Phoenix - delivers transcutaneous auricular vagal nerve stimulation (taVNS) in a discreet earbud design. Pairing the Phoenix with our PTSD symptom tracking app will allow for reimbursable remote clinician monitoring and the establishment of a leading PTSD database collecting biosignals, symptoms, and therapy effectiveness.

7.5 million Americans seek treatment for PTSD every year and the rates tripled during the COVID shutdown. The current standard of care also leaves a 66% unmet medical need in this $8 billion market. The Phoenix is an earbud that provides personalized medicine that addresses the underlying autonomic imbalance of PTSD by delivering transcutaneous auricular vagal nerve stimulation (taVNS) in a proprietary closed-loop system.

"Evren is committed to human centered design for our Phoenix earbud, as well as pursuing sound clinical research to prove the benefits, useability, safety, and effectiveness of our technology," said Blythe Karow, Co-founder & CEO of Evren. "We look forward to our pivotal trial next year and to applying for marketing approval under the De Novo Classification program."

"We are grateful for the recognition by the FDA of the potential for this novel Phoenix device," said Donna DiGangi of DiGangi Consulting, LLC and Evren's regulatory advisor. "We appreciated the FDA's responsiveness as we replied to their key questions, allowing us to secure this designation."

The goal of the Breakthrough Designation Program is to help speed the development and shorten review time of medical devices with the potential to provide more effective treatment for life-threatening or irreversibly debilitating diseases. A key requirement for the Designation is preliminary clinical evidence demonstrating substantial improvement on a clinically significant endpoint compared with other available therapies. In addition, there are government policies under consideration that, if eventually adopted, may facilitate Medicare reimbursement for FDA Breakthrough Devices following marketing authorization.

About Evren Technologies

Evren Technologies is advancing the treatment of PTSD through an easy-to-use platform. The Phoenix® medical device provides personalized medicine in a discreet earbud design that delivers transcutaneous auricular vagal nerve stimulation (taVNS). Pairing the Phoenix with our PTSD symptom tracking app allows for reimbursable remote clinician monitoring and the establishment of a leading PTSD database that collects biosignals, symptom tracking, triggering events, and therapy effectiveness. 

Media and Investors:

Interviews, Images, Video Clips available on request.

M. Blythe Karow
Co-founder & CEO
352.533.3381 x702
blythe.karow@evrenvns.com  

 

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SOURCE Evren Technologies

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