Hager& Meisinger GmbH

Hager& Meisinger GmbH — FDA 510(k) Submissions

Hager& Meisinger GmbH has submitted 14 FDA 510(k) premarket notifications since 2007, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Screw, Fixation, Intraosseous, Abutment, Implant, Dental, Endosseous, Forceps, Tooth Extractor, Surgical . Use the specialty filter in the sidebar to narrow results.