FDA applicant
Air Liquide Healthcare America
FDA records 4 decisions for Air Liquide Healthcare America (Houston, TX) from 2006 to 2017: 4 510(k) clearances. Most are in product codes ECX (Cylinder, Compressed Gas, And Valve) and GEX (Powered Laser Surgical Instrument). Its devices cite 4 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Air Liquide Healthcare America Corporation”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Air Liquide Healthcare America’s devices, and how often a recall has named them.
FDA decisions per year
1in 2017
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Air Liquide Healthcare America’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report