Iridex Corp - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Iridex Corp — FDA 510(k) Products and Clearance History General & Plastic Surgery ✕
9 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 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
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
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