FDA applicant

Linde Gas North America, LLC

Murray Hill, NJ1 decision2011–20110 recalls

FDA records 1 decision for Linde Gas North America, LLC (Murray Hill, NJ) in 2011: 1 510(k) clearance. All are in product code ECX (Cylinder, Compressed Gas, And Valve). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

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 Linde Gas North America, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Linde Gas North America, LLC by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Linde”

FDA records each applicant name separately; these may or may not be the same firm.

Linde Div. Union Carbide Corp. 6 Linde Medical Sensors AG 4 Linde Gas & Equipment, Inc. 3 Linde Gas Therapeutics 2 Linde Healthcare AB 1

Linde Gas North America, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Linde”