FDA applicant

Myo/Kinetic Systems, Inc.

Menomonee Falls, WI8 decisions1992–19950 recalls

FDA records 8 decisions for Myo/Kinetic Systems, Inc. (Menomonee Falls, WI) from 1992 to 1995: 8 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and KPI (Stimulator, Electrical, Non-Implantable, For…). 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/Kinetic Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Myo/Kinetic Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Myo/Kinetic Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?