Bausch & Lomb is one of 13008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bausch & Lomb - FDA 510(k) Cleared Devices
Recent clearances: Stellaris Elite vision enhancement system, Stellaris Elite Vision Enhancement System, STELLARIS PC VISION ENHANCEMENT SYSTEM
12
Total
12
Cleared
0
Denied
Bausch & Lomb has 12 FDA 510(k) cleared ophthalmic devices. Based in Rochester, US.
Historical record: 12 cleared submissions from 2002 to 2017.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bausch+Lomb as regulatory consultant.
FDA 510(k) Regulatory Record - Bausch & Lomb
12 devices
Cleared
Apr 19, 2017
Stellaris Elite vision enhancement system
Ophthalmic
104d
Cleared
Mar 24, 2017
Stellaris Elite Vision Enhancement System
Ophthalmic
214d
Cleared
Mar 12, 2014
STELLARIS PC VISION ENHANCEMENT SYSTEM
Ophthalmic
119d
Cleared
Feb 14, 2014
STELLARIS VISION ENHANCEMENT SYSTEM
Ophthalmic
116d
Cleared
Jan 09, 2014
BAUSCH & LOMB INJECTOR SYSTEM
Ophthalmic
196d
Cleared
Jan 03, 2014
BAUSCH + LUMB, VIS100 INJECTOR SYSTEM
Ophthalmic
78d
Cleared
Dec 27, 2013
EASY-LOAD LENS DELIVERY SYSTEM
Ophthalmic
141d
Cleared
Sep 17, 2013
CRYSTALSERT DELIVERY SYSTEM
Ophthalmic
29d
Cleared
May 16, 2013
CRYSTALSERT DELIVERY SYSTEM
Ophthalmic
162d
Cleared
Jun 22, 2006
SOFLENS ONE DAY PLUS DISPOSABLE (HILAFILCON B) VISIBILITY TINTED CONTACT LENS
Ophthalmic
57d
Cleared
Jul 23, 2004
NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)
Ophthalmic
106d
Cleared
May 16, 2002
BAUSCH & LOMB SOFLENS MULTIFOCAL (POLYMACON) VISIBILITY TINTED CONTACT LENS
Ophthalmic
56d