# Air Liquide Healthcare America

- Location (FDA's records): Houston, TX
- FDA decisions: 4 (2006–2017): 4 510(k) clearances
- Names in FDA's records: Air Liquide Healthcare America (2); Air Liquide Healthcare America Corporation (2)
- Product codes: ECX (3), GEX (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 4 (1 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
- Candela Corp.: 1 (https://510kreport.com/company/candela)
- Aga-Linde Health Care: 1 (https://510kreport.com/company/aga-linde-health-care)
- Air Liquide Healthcare: 1 (https://510kreport.com/company/air-liquide-healthcare)

## Firms that cite its devices most
- Western/Scott Fetzer Co.: 1 (https://510kreport.com/company/western-scott-fetzer)
- Air Liquide Healthcare: 1 (https://510kreport.com/company/air-liquide-healthcare)
- San Cheong Co., Ltd.: 1 (https://510kreport.com/company/san-cheong)

## Its most-cited devices
- K053117: EZ-OX Plus (2006), cited by 3
- K131386: EZ-OX Plus Generation II (2014), cited by 1

## Recent decisions
- K161179: Intelli-Ox (Apr 13, 2017)
- K153564: Pure Cryogen (Mar 29, 2016)
- K131386: EZ-OX Plus Generation II (Mar 14, 2014)
- K053117: EZ-OX Plus (Apr 10, 2006)

Source page: https://510kreport.com/company/air-liquide-healthcare-america