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

Bausch & Lomb, Incorporated has 27 FDA 510(k) cleared ophthalmic devices. Based in Rochester, US.

Latest FDA clearance: Oct 2024. Active since 2002.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Bausch + Lomb, Incorporated and Eyereg Consulting, Inc.. 4 devices have linked clinical trials registered on ClinicalTrials.gov.