510(k) Report

FDA applicant

Acetylene Gas Co.

St. Louis, MO3 decisions1993–19940 recalls

FDA records 3 decisions for Acetylene Gas Co. (St. Louis, MO) from 1993 to 1994: 3 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and BZC (Calculator, Pulmonary Function Data). 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 Acetylene Gas Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Acetylene Gas Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Acetylene Gas Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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