FDA applicant

Maximum Performance Technologies, Mpts, Inc.

Washington, D.C., DC11 decisions1990–19910 recalls

FDA records 11 decisions for Maximum Performance Technologies, Mpts, Inc. (Washington, D.C., DC) from 1990 to 1991: 11 510(k) clearances. All are in product code IPF (Stimulator, Muscle, Powered). 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 Maximum Performance Technologies, Mpts, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Maximum Performance Technologies, Mpts, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Maximum Performance Technologies, Mpts, Inc.

Which product codes does it file in?

What has FDA decided for it lately?