Synthes GmbH

Synthes GmbH — FDA 510(k) Submissions

Synthes GmbH has submitted 7 FDA 510(k) premarket notifications since 2024, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Fixation, Bone, Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, Plate, Cranioplasty, Preformed, Non-alterable . Use the specialty filter in the sidebar to narrow results.