FDA applicant

General Physiotherapy, Inc.

St. Louis, MO9 decisions1981–19870 recalls

FDA records 9 decisions for General Physiotherapy, Inc. (St. Louis, MO) from 1981 to 1987: 9 510(k) clearances. Most are in product codes ISA (Massager, Therapeutic, Electric) and IRO (Vibrator, Therapeutic). 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 General Physiotherapy, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for General Physiotherapy, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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General Physiotherapy, Inc.

Which product codes does it file in?

What has FDA decided for it lately?