Medical Device Manufacturer · US , Mountain View , CA

Iriderm Div. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1989

Recent clearances: DIOLITE 532, OCULIGHT GL, DIOPEXY PROBE

10

Total

10

Cleared

0

Denied

FDA 510(k) Regulatory Record - Iriderm Div. General & Plastic Surgery ✕

8 devices

1-8 of 8

Cleared Apr 01, 1997

General & Plastic Surgery · 172d

Cleared Jul 28, 1994

General & Plastic Surgery · 979d

Cleared Apr 19, 1994

D'AMICO\PEYMAN FLUTED ENDOPROBE

General & Plastic Surgery · 350d

Cleared Aug 11, 1992

IRIS OCULIGHT SL

General & Plastic Surgery · 82d

Cleared Nov 15, 1991

IRIS OCULIGHT(R) SLX

General & Plastic Surgery · 106d

Cleared Aug 23, 1991

IRIS OCULIGHT DIODE LASER ADDING SLIT LAMP ADAPTER

General & Plastic Surgery · 51d

Cleared Sep 24, 1990

IRIS OCULIGHT SL DIODE LASER PHOTOCOAG/MODIFIED

General & Plastic Surgery · 88d

Cleared Oct 05, 1989

IRIS OCULIGHT(TM) SL

General & Plastic Surgery · 66d