Ipax, Inc.
Ipax, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2021.
Top product codes for Ipax, Inc.
Recent clearances by Ipax, Inc.
- K200893 — ProntoPump Sterile Tube Set
- K971242 — BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28)
- K971245 — BLINK EXTERNAL EYELID WEIGHT
- K915158 — SUREBREATH DOME, E-Z BREATHER
- K915118 — PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBE
- K914172 — KPE 230 AM
- K914221 — KPE 220 TS, NONSTERILE
- K884076 — SUREBREATH DOME
- K873097 — PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKS
- K870770 — TIMLEINE(TM) VENIPUNCTURE SYSTEM
- K864726 — I/A/KPE TIP
- K863729 — OPHTHALMIC FITLER MICRO CAPSULE
- K863209 — US PLUS-PAK(R) SURGICAL SYSTEM
- K862334 — CATALOG NO. I/A 100 AND KPE 200
- K860609 — TIMELINE VENIPUNCTURE SYSTEM
- K861182 — TIMELINE VENIPUNCTURE SYSTEM
- K833961 — I/A PLUS PAK SURGICAL SYSTEM
- K833962 — KPE PLUS-PAK SURGICAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.