Bausch and Lomb - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bausch and Lomb has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bausch and Lomb Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Bausch and Lomb
1 devices