Luxottica Group S.P.A. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Luxottica Group S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: Nuance Audio Hearing Aid Software
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) Regulatory Record - Luxottica Group S.P.A.
1 devices