Cochlear

Cochlear — FDA 510(k) Submissions

Cochlear has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, Active Implantable Bone Conduction Hearing System, Hearing Aid, Bone Conduction . Use the specialty filter in the sidebar to narrow results.