Bausch and Lomb is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bausch and Lomb - FDA 510(k) Cleared Devices
Recent clearances: Stellaris Elite™ vision enhancement system, Stellaris Elite vision enhancement system
2
Total
2
Cleared
0
Denied
Bausch and Lomb has 2 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Latest FDA clearance: May 2026. 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) Regulatory Record - Bausch and Lomb
2 devices