FDA applicant

Linde Gas & Equipment, Inc.

Livingston, TN3 decisions2022–20244 recalls

FDA records 3 decisions for Linde Gas & Equipment, Inc. (Livingston, TN) from 2022 to 2024: 3 510(k) clearances. All are in product code MRN (Apparatus, Nitric Oxide Delivery). Its devices cite 4 predicates, 2 of them its own earlier devices. 4 recalls are linked to its devices, 2 Class I.

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 & Equipment, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2022high 1 (2022) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

2in 2026

2022high 2 (2025) · low 0 (2022)2026

Class I Class II/III not classified

FIG. 1 — Linde Gas & Equipment, Inc. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Linde Gas & Equipment, Inc.’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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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 Therapeutics 2 Linde Healthcare AB 1 Linde Gas North America, LLC 1

Linde Gas & Equipment, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Linde”