Bausch & Lomb, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Bausch + Lomb PreVue Inserter for enVista Preloaded, Crystalsert Lens Delivery System, Bausch + Lomb Injector System
92
Total
92
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bausch & Lomb, Inc. Pathology ✕
1 devices