Luxottica Group S.P.A. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Luxottica Group S.P.A. has 1 FDA 510(k) cleared medical devices. Based in Milan, IT.
Latest FDA clearance: Jan 2025. Active since 2025. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Luxottica Group S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Luxottica Group S.P.A.
1 devices