Medical Device Manufacturer · US , Rodchester , NY

Bausch and Lomb, Incorporated - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2018

Total

Cleared

Denied

Bausch and Lomb, Incorporated has 3 FDA 510(k) cleared medical devices. Based in Rodchester, US.

Latest FDA clearance: Mar 2026. Active since 2018. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Bausch and Lomb, Incorporated Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Bausch and Lomb, Incorporated

3 devices

1-3 of 3