Heraeus Kulzer,GmbH

Heraeus Kulzer,GmbH — FDA 510(k) Submissions

Heraeus Kulzer,GmbH has submitted 10 FDA 510(k) premarket notifications since 2004, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Bone Cement, Material, Tooth Shade, Resin, Agent, Tooth Bonding, Resin, Material, Impression, Alloy, Gold-based Noble Metal . Use the specialty filter in the sidebar to narrow results.