FDA applicant

Linde Div. Union Carbide Corp.

Somerset, NJ6 decisions1982–19880 recalls

FDA records 6 decisions for Linde Div. Union Carbide Corp. (Somerset, NJ) from 1982 to 1988: 6 510(k) clearances. Most are in product codes GCX (Apparatus, Suction, Operating-Room, Wall…) and CHL (Electrode Measurement, Blood-Gases (Pco2, Po2)…). 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 Div. Union Carbide Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Linde Div. Union Carbide Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Linde Div. Union Carbide Corp. by year, 2007–2026Sources: 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 Medical Sensors AG 4 Linde Gas & Equipment, Inc. 3 Linde Gas Therapeutics 2 Linde Healthcare AB 1 Linde Gas North America, LLC 1

Linde Div. Union Carbide Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Linde”