Medical Device Manufacturer · DE , Pullach

Adeor Medical Technologies GmbH

1 submissions · 1 cleared · Since 2012
1
Total
1
Cleared
0
Denied

Adeor Medical Technologies GmbH — FDA 510(k) Submissions

Adeor Medical Technologies GmbH has submitted 1 FDA 510(k) premarket notifications since 2012, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drills, Burrs, Trephines & Accessories (compound, Powered) . Use the specialty filter in the sidebar to narrow results.

1 devices
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