FDA applicant

Thermionics Corp.

Springfield, IL1 decision1992–19920 recalls

FDA records 1 decision for Thermionics Corp. (Springfield, IL) in 1992: 1 510(k) clearance. All are in product code IME (Pack, Hot Or Cold, Reusable). 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, physical medicine panel, where it files most

How often FDA has decided Thermionics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Thermionics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Thermionics Corp.

Which product codes does it file in?

What has FDA decided for it lately?