Medical Device Manufacturer · US , CO

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

18 submissions · 18 cleared · Since 1984

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) cleared devices by 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