Med-El Elektromedizinische Ger?te GmbH

Med-El Elektromedizinische Ger?te GmbH — FDA 510(k) Submissions

Med-El Elektromedizinische Ger?te GmbH has submitted 3 FDA 510(k) premarket notifications since 2025, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Partial Ossicular Replacement, Replacement, Ossicular Prosthesis, Total . Use the specialty filter in the sidebar to narrow results.