FDA applicant

T. G. & E. Medical

Mchenry, IL5 decisions1982–19860 recalls

FDA records 5 decisions for T. G. & E. Medical (Mchenry, IL) from 1982 to 1986: 5 510(k) clearances. Most are in product codes KPD (Strip, Temperature, Forehead, Liquid Crystal) and CAT (Cannula, Nasal, Oxygen). 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, general hospital panel, where it files most

How often FDA has decided T. G. & E. Medical’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for T. G. & E. Medical since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — T. G. & E. Medical by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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T. G. & E. Medical

Which product codes does it file in?

What has FDA decided for it lately?