Medical Device Manufacturer · DE , Bremen

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

4 submissions · 4 cleared · Since 1998
4
Total
4
Cleared
0
Denied

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO — FDA 510(k) Submissions

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO has submitted 4 FDA 510(k) premarket notifications since 1998, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powder, Porcelain, Alloy, Metal, Base, Alloy, Other Noble Metal . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Dental 4