Medical Device Manufacturer · BE , Herstal

Cefaly Technology - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2016

Total

Cleared

Denied

Cefaly Technology has 6 FDA 510(k) cleared medical devices. Based in Herstal, BE.

Latest FDA clearance: Jul 2024. Active since 2016. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Cefaly Technology Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Elexes Medical Consulting, LLC and Elexes Medical Consulting.

Cefaly Technology is one of 33 FDA 510(k) medical device manufacturers from Belgium in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cefaly Technology

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 10, 2026