# Ipax, Inc.

- Location (FDA's records): Englewood, CO
- FDA decisions: 18 (1984–2021): 18 510(k) clearances
- Product codes: HQC (7), GAD (2), FPA (2), MML (2), HQE (1), GBQ (1), KMK (1), LHI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Baxa Corp.: 1 (https://510kreport.com/company/baxa)

## Recent decisions
- K200893: ProntoPump Sterile Tube Set (May 4, 2021)
- K971242: Blink Gold Evelid Weight (BG 06 Thru BG 28) (Dec 17, 1997)
- K971245: Blink External Eyelid Weight (Jun 20, 1997)
- K915158: Surebreath Dome, E-Z Breather (Feb 12, 1992)
- K915118: Phaco Emulsification,Irrigation/Aspiration Tube (Dec 27, 1991)
- K914172: KPE 230 AM (Oct 25, 1991)
- K914221: Kpe 220 TS, Nonsterile (Oct 25, 1991)
- K884076: Surebreath Dome (Oct 7, 1988)

Source page: https://510kreport.com/company/ipax