Bausch & Lomb, Incorporated - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
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.
FDA 510(k) cleared devices by Bausch & Lomb, Incorporated
27 devices
Cleared
Oct 10, 2024
EyeGility™ Inserter for Preloaded enVista IOLs
Ophthalmic
59d
Cleared
Nov 17, 2023
Samfilcon B Custom Contact Lens
Ophthalmic
227d
Cleared
Mar 08, 2023
Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens, Bausch + Lomb...
Ophthalmic
370d
Cleared
Dec 06, 2022
Bausch + Lomb Preservative Free Lubricating and Rewetting Drops
Ophthalmic
106d
Cleared
Dec 03, 2021
Independent Corneal Viewing Chamber (IVC-21)
Ophthalmic
177d
Cleared
May 28, 2021
ABT12 multi-purpose solution
Ophthalmic
241d
Cleared
May 24, 2021
Bausch + Lomb (kalifilcon A) Soft (hydrophilic) Contact Lens for Presbyopia
Ophthalmic
53d
Cleared
Sep 23, 2020
Boston One Step Liquid Enzymatic Cleaner
Ophthalmic
216d
Cleared
Jun 02, 2020
Bausch + Lomb (Kalifilcon A) Soft Contact Lens, Bausch + Lomb (Kalifilcon A)...
Ophthalmic
92d
Cleared
Feb 12, 2019
Boston ES (enflufocon A) Rigid Gas Permeable Contact Lens
Ophthalmic
89d
Cleared
Nov 30, 2018
Ultra (samfilcon A) Multifocal for Astigmatism Contact Lens
Ophthalmic
102d
Cleared
Aug 10, 2018
Bausch + Lomb Boston SimplusMulti-Action Solution, Bausch + Lomb Boston One...
Ophthalmic
51d