Medical Device Manufacturer · BE , Herstal

Cefaly Technology - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2016
6
Total
6
Cleared
0
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.

FDA 510(k) Regulatory Record - Cefaly Technology
6 devices
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