FDA applicant

Myo-Tronics, Inc.

Seattle, WA6 decisions1991–19970 recalls

FDA records 6 decisions for Myo-Tronics, Inc. (Seattle, WA) from 1991 to 1997: 6 510(k) clearances. Most are in product codes KZM (Device, Muscle Monitoring) and NFQ (Device, Dental Sonography, For Monitoring Jaw…). 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, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Myo-Tronics, 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?