Medical Device Manufacturer · US , CO

Ipax, Inc. - FDA 510(k) Cleared Devices

18 submissions · 18 cleared · Since 1984

Recent clearances: ProntoPump Sterile Tube Set

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.

Ipax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ipax, Inc.

18 devices

1-12 of 18

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

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

Ophthalmic · 85d

Cleared Oct 10, 1986

OPHTHALMIC FITLER MICRO CAPSULE

Ophthalmic · 17d