Merz Dental GmbH

Merz Dental GmbH — FDA 510(k) Submissions

Merz Dental GmbH has submitted 9 FDA 510(k) premarket notifications since 2003, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Crown And Bridge, Temporary, Resin, Denture, Plastic, Teeth, Resin, Denture, Relining, Repairing, Rebasing, Mouthguard, Prescription, Material, Tooth Shade, Resin . Use the specialty filter in the sidebar to narrow results.