Medical Device Manufacturer · US , Danville , CA

Brainbase Corporation

3 submissions · 3 cleared · Since 2006
3
Total
3
Cleared
0
Denied

Brainbase Corporation — FDA 510(k) Submissions

Brainbase Corporation has submitted 3 FDA 510(k) premarket notifications since 2006, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Airbrush, Bone Grafting Material, Synthetic . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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