Bausch & Lomb, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Bausch + Lomb PreVue Inserter for enVista Preloaded, Crystalsert Lens Delivery System
92
Total
92
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bausch & Lomb, Inc. Ophthalmic ✕
76 devices
Cleared
Oct 04, 2019
Bausch + Lomb PreVue Inserter for enVista Preloaded
Ophthalmic
67d
Cleared
Dec 11, 2017
Crystalsert Lens Delivery System
Ophthalmic
28d
Cleared
May 22, 2015
Bausch + Lomb Injector System
Ophthalmic
28d
Cleared
Sep 11, 2013
BAUSCH + LOMB PROCOMFORT (SAMFILCON A) CONTACT LENS, BAUSCH + LOMB PROCOMFORT...
Ophthalmic
135d
Cleared
Dec 20, 2012
BAUSCH & LOMB PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS,...
Ophthalmic
119d
Cleared
Sep 28, 2012
BAUSCH & LOMB IOL INJECTOR
Ophthalmic
274d
Cleared
Apr 30, 2012
OCD04 3% HYDROGEN PEROXIDE CLEANING AND DISINFECTING SOULTION
Ophthalmic
210d
Cleared
Jan 24, 2012
EZS05 CLEANING AND DISINFECTING SOLUTION, BAUSCH + LOMB EZS05 CLEANING AND...
Ophthalmic
207d
Cleared
Oct 25, 2011
NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS
Ophthalmic
88d
Cleared
Aug 17, 2010
STELLARIS PC VISION ENHANCEMENT SYSTEM
Ophthalmic
97d
Cleared
Nov 18, 2009
BPZ02 MULTIPURPOSE SOLUTION
Ophthalmic
336d
Cleared
Jan 05, 2009
BAUSCH & LOMB STELLARIS MICROSURGICAL SYSTEM
Ophthalmic
131d
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