Medical Device Manufacturer · DE , Valley

Adeor Medical AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Adeor Medical AG has 4 FDA 510(k) cleared medical devices. Based in Valley, DE.

Latest FDA clearance: Mar 2026. Active since 2014. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Adeor Medical AG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Adeor Medical AG

4 devices

1-4 of 4