510(k) Report

FDA applicant

Air Liquide Healthcare America

Houston, TX4 decisions2006–20170 recalls

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, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

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

2014: 12016: 12017: 1
2007high 1 (2014) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Air Liquide Healthcare America by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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