Ipax, Inc. is one of 16315 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ipax, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ProntoPump Sterile Tube Set, BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28), BLINK EXTERNAL EYELID WEIGHT
18
Total
18
Cleared
0
Denied
Ipax, Inc. has 18 FDA 510(k) cleared medical devices. Based in US.
Last cleared in 2021. Active since 1984. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ipax, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ipax, Inc.
18 devices
Cleared
May 04, 2021
ProntoPump Sterile Tube Set
General Hospital
396d
Cleared
Dec 17, 1997
BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28)
Ophthalmic
259d
Cleared
Jun 20, 1997
BLINK EXTERNAL EYELID WEIGHT
Ophthalmic
78d
Cleared
Feb 12, 1992
SUREBREATH DOME, E-Z BREATHER
General & Plastic Surgery
90d
Cleared
Dec 27, 1991
PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBE
Ophthalmic
44d
Cleared
Oct 25, 1991
KPE 230 AM
Ophthalmic
60d
Cleared
Oct 25, 1991
KPE 220 TS, NONSTERILE
Ophthalmic
63d
Cleared
Oct 07, 1988
SUREBREATH DOME
General & Plastic Surgery
10d
Cleared
Sep 04, 1987
PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKS
General & Plastic Surgery
39d
Cleared
Apr 23, 1987
TIMLEINE(TM) VENIPUNCTURE SYSTEM
General Hospital
56d
Cleared
Jan 20, 1987
I/A/KPE TIP
Ophthalmic
85d
Cleared
Oct 10, 1986
OPHTHALMIC FITLER MICRO CAPSULE
Ophthalmic
17d