Luxottica Group S.P.A.

Luxottica Group S.P.A. — FDA 510(k) Submissions

Luxottica Group S.P.A. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Air-conduction Hearing Aid Software . Use the specialty filter in the sidebar to narrow results.