Alcon Research, Ltd. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Alcon Research, Ltd. Ophthalmic ✕
14 devices
Cleared
Apr 14, 2017
CENTURION Vision System (Active SentryTM)
Ophthalmic
288d
Cleared
Mar 22, 2017
HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit...
Ophthalmic
28d
Cleared
Aug 22, 2014
CONSTELLATION VISION SYSTEM
Ophthalmic
120d
Cleared
Mar 27, 2012
MONARCH III IOL DELIVERY SYSTEM, MONARCH III C CARTRIDGE, MONARCH III...
Ophthalmic
173d
Cleared
Oct 17, 2011
27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+...
Ophthalmic
196d
Cleared
May 20, 2011
CLEARCUT S SAFETY KNIFE
Ophthalmic
120d
Cleared
May 10, 2011
ALCON MULTI-PIRPOSE DISINFECTING SOLUTION
Ophthalmic
222d
Cleared
Apr 02, 2010
ENHANCED ULTRA VIT PROBE
Ophthalmic
162d
Cleared
Oct 20, 2009
ALCON ULTRACHOPPER
Ophthalmic
125d
Cleared
Feb 12, 2009
INFINITI VISION SYSTEM WITH OZIL IP
Ophthalmic
139d
Cleared
Nov 08, 2006
LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
Ophthalmic
41d
Cleared
Sep 14, 2005
ALCON MULTI-PURPOSE DISINFECTING SOLUTION
Ophthalmic
177d