Medical Device Manufacturer · US , Bonita Springs , FL

Biegler GmbH

3 submissions · 3 cleared · Since 2012
3
Total
3
Cleared
0
Denied

Biegler GmbH — FDA 510(k) Submissions

Biegler GmbH has submitted 3 FDA 510(k) premarket notifications since 2012, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Electro-acupuncture, Warmer, Thermal, Infusion Fluid . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Neurology 2 General Hospital 1