Medical Device Manufacturer · AT , Burmoos

W&H Dentalwerk Buermoss GmbH

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

W&H Dentalwerk Buermoss GmbH — FDA 510(k) Submissions

W&H Dentalwerk Buermoss GmbH has submitted 2 FDA 510(k) premarket notifications since 2022, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Drill, Surgical, Ent (electric Or Pneumatic) Including Handpiece, Scaler, Ultrasonic . Use the specialty filter in the sidebar to narrow results.

2 devices
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