Iridex Corp is one of 5407 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iridex Corp - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Iridex Corp has 13 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 13 cleared submissions from 1998 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Iridex Corp Filter by specialty or product code using the sidebar.
Iridex Corp — FDA 510(k) Products and Clearance History
13 devices
Cleared
Nov 28, 2012
TXCELL SCANNING LASER DELIVERY SYSTEM
General & Plastic Surgery
194d
Cleared
Aug 07, 2008
FAMILI OF IRIDEX IQ LASER SYSTEMS
General & Plastic Surgery
416d
Cleared
Nov 14, 2006
IRIDEX WIRELESS FOOTSWITCH
Ophthalmic
116d
Cleared
Nov 08, 2006
IRIDEX OCULIGHT TX
General & Plastic Surgery
86d
Cleared
May 31, 2006
IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1
General & Plastic Surgery
58d
Cleared
Apr 14, 2005
OCULIGHT GL/GLX
General & Plastic Surgery
42d
Cleared
Sep 20, 2004
IRIS MEDICAL IQ 810 PHOTOCOAGULATOR
Ophthalmic
234d
Cleared
Aug 27, 2003
IRIS MEDICAL OCULIGHT GL/GLX LASER SYSTEMS
Ophthalmic
90d
Cleared
Oct 08, 2002
FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES
General & Plastic Surgery
90d
Cleared
May 20, 2002
APEX 800 LASER SYSTEM, MODEL APEX 800
General & Plastic Surgery
66d
Cleared
May 03, 2002
OCULIGHT SL/SLX
Ophthalmic
88d
Cleared
Dec 09, 1999
IRIDERM, MODEL APEX 800
General & Plastic Surgery
154d
Cleared
Sep 08, 1998
OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE
General & Plastic Surgery
90d