Medical Device Manufacturer · DE , Baden-Wurttemberg

Vita Zahnfabrik H. Rauter GmbH & Co. Kg.

2 submissions · 2 cleared · Since 2009
2
Total
2
Cleared
0
Denied

Vita Zahnfabrik H. Rauter GmbH & Co. Kg. — FDA 510(k) Submissions

Vita Zahnfabrik H. Rauter GmbH & Co. Kg. has submitted 2 FDA 510(k) premarket notifications since 2009, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powder, Porcelain, Agent, Tooth Bonding, Resin . Use the specialty filter in the sidebar to narrow results.

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