FDA applicant

Myo-Tronics Research, Inc.

Mchenry, IL8 decisions1977–19840 recalls

FDA records 8 decisions for Myo-Tronics Research, Inc. (Mchenry, IL) from 1977 to 1984: 8 510(k) clearances. Most are in product codes NUW (Stimulator, Muscle, Powered, Dental) and KZM (Device, Muscle Monitoring). 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 Myo-Tronics Research, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Myo-Tronics Research, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Myo-Tronics Research, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?