Medical Device Manufacturer · DE , Ettingen

Detax GmbH

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

Detax GmbH — FDA 510(k) Submissions

Detax GmbH has submitted 3 FDA 510(k) premarket notifications since 2022, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Tooth Shade, Resin, Mouthguard, Prescription, Resin, Denture, Relining, Repairing, Rebasing . Use the specialty filter in the sidebar to narrow results.

3 devices
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