• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to footer

MassDevice

The Medical Device Business Journal — Medical Device News & Articles | MassDevice

  • Special Reports
  • Technologies
    • Artificial Intelligence (AI)
    • Cardiovascular
    • Orthopedics
    • Neurological
    • Diabetes
    • Surgical Robotics
  • Business & Finance
    • Wall Street Beat
    • Earnings Reports
    • Funding Roundup
    • Mergers & Acquisitions
    • Initial Public Offering (IPO)
    • Legal News
    • Personnel Moves
    • Medtech 100 Stock Index
  • Regulatory
    • Food & Drug Administration (FDA)
    • Recalls
    • 510(k)
    • Pre-Market Approval (PMA)
    • MDSAP
    • Clinical Trials
  • Resources
    • About MassDevice
    • Leadership in Medtech
    • Manufacturers & Suppliers Search
    • MedTech100 Index
    • Videos
    • Webinars
    • Whitepapers
    • Voices
    • In-Depth Coverage
    • Latest News
  • Attend DeviceTalks
    • Events
      • DeviceTalks Minnesota – May 4
      • DeviceTalks Boston – May 27–28
      • DeviceTalks West
      • DeviceTalks Tuesdays
    • DeviceTalks Podcast Network
      • DeviceTalks Weekly
      • AbbottTalks
      • Boston ScientificTalks
      • DeviceTalks AI
      • IntuitiveTalks
      • MedtechWOMEN Talks
      • MedtronicTalks
      • Neuro Innovation Talks
      • Ortho Innovation Talks
      • Structural Heart Talks
      • StrykerTalks
  • Advertise
  • Subscribe
Home » FDA clears Neurolief’s noninvasive neuromod tech to treat migraines

FDA clears Neurolief’s noninvasive neuromod tech to treat migraines

March 2, 2021 By Danielle Kirsh

Neurolief Relivion noninvasive neuromodulation system migraines
The Relivion noninvasive neuromodulation system to treat migraines [Image courtesy of Neurolief]
Neurolief today announced that it received FDA clearance for its Relivion noninvasive neuromodulation system to treat migraines.

The noninvasive, multi-channel brain neuromodulation system’s creators designed it to treat acute migraines from home. It is a headset that administers personalized care to patients by delivering stimulation to six branches of the occipital and trigeminal nerves through three adaptive output channels. The output channels allow for the release of neurotransmitters in the brainstem and the modulation of brain networks associated with pain control.

“The FDA clearance of the Relivion noninvasive device is an important event for those suffering from migraines, as it is the only neuromodulation technology thus far that has demonstrated statistically significant efficacy in providing complete freedom of migraine symptoms within 2 hours after treatment, in a sham-controlled clinical trial,” principal investigator on the pivotal international trial Stewart Tepper said in a news release.

“Patients will now have access to a highly effective, easy-to-use, non-invasive, and drug-free therapeutic option that will help them regain control of their lives,” Tepper said.

The FDA clearance is based on a multi-center, prospective, randomized, double-blind, placebo-controlled clinical study. In the study, 46% of patients in the active group were pain-free, compared to only 11.8% of patients in the control group, according to the company. 75% of patients in the active group had complete freedom from the most bothersome symptoms (photophobia, photophobia or nausea) within two hours of treatment.

“This is a major milestone both for Neurolief and the migraine community. Relivion offers a new paradigm for doctors treating migraine patients, reducing the dependence on pharmaceutical products and invasive procedures while keeping doctors informed of the patient’s progress,” Neurolief board chair Chris Richardson said in a news release. “It also demonstrates our commitment to becoming the leader in neuromodulation therapy and allows a springboard to advance this technology in the future for other neurological and neuropsychiatric disorders.”

Filed Under: Featured, Neuromodulation/Neurostimulation, Pain Management Tagged With: Neurolief

More recent news

  • Abbott sets Libre Duo glucose-ketone sensor US launch for December
  • Edwards wins FDA approval for Pascal Precision in tricuspid valve repair
  • Danaher’s Masimo acquisition offsets drops in respiratory diagnostic sales
  • Intuitive stock slides as US procedures slow amid $450M settlement
  • Abbott to spin out Nutrition business, cuts guidance

About Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at [email protected].

Primary Sidebar

“md
EXPAND YOUR KNOWLEDGE AND STAY CONNECTED
Get the latest med device regulatory, business and technology news.

DeviceTalks Weekly

See More >
MDO ad
MDO ad

Footer

MASSDEVICE MEDICAL NETWORK

DeviceTalks
Drug Delivery Business News
Medical Design & Outsourcing
Medical Tubing + Extrusion
Drug Discovery & Development
Pharmaceutical Processing World
MedTech 100 Index
R&D World
Medical Design Sourcing

DeviceTalks Webinars, Podcasts, & Discussions

Attend our Monthly Webinars
Listen to our Weekly Podcasts
Join our DeviceTalks Tuesdays Discussion

MASSDEVICE

Subscribe to MassDevice E-Newsletter
Advertise with us
About
Contact us

Copyright © 2026 · Arrowfly LLC and its licensors. All rights reserved.
The material on this site may not be reproduced, distributed, transmitted, cached or otherwise used, except with the prior written permission of Arrowfly.

Privacy Policy