FDA applicant

Mon-A-Therm, Inc.

St. Louis, MO17 decisions1982–19890 recalls

FDA records 17 decisions for Mon-A-Therm, Inc. (St. Louis, MO) from 1982 to 1989: 17 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and GEI (Electrosurgical, Cutting & Coagulation &…). 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 Mon-A-Therm, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mon-A-Therm, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Mon-A-Therm, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Mon-A-Therm, Inc.

Which product codes does it file in?

What has FDA decided for it lately?