Alcon Research, Ltd. is one of 4724 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alcon Research, Ltd. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Alcon Research, Ltd. has 16 FDA 510(k) cleared ophthalmic devices. Based in Fort Worth, US.
Historical record: 16 cleared submissions from 2000 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.
FDA 510(k) Regulatory Record - Alcon Research, Ltd.
16 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
Jun 21, 2012
WAVELIGHT FS200 PATIENT INTERFACE 1505
General & Plastic Surgery
77d
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
Oct 21, 2010
WAVELIGHT FS200 LASER SYSTEM MODEL: FS200
General & Plastic Surgery
192d
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