Iriderm Div. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Iriderm Div. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Iriderm Div. has 10 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 10 cleared submissions from 1989 to 1997.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Iriderm Div.
10 devices
Cleared
Apr 01, 1997
DIOLITE 532
General & Plastic Surgery
172d
Cleared
Aug 28, 1996
OCULIGHT GL
Ophthalmic
170d
Cleared
Jul 19, 1996
DIOPEXY PROBE
Ophthalmic
164d
Cleared
Jul 28, 1994
IRIS G-PROBE
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