FDA applicant

Universal Technology Systems, Inc.

Jacksonville, FL3 decisions1990–19980 recalls

FDA records 3 decisions for Universal Technology Systems, Inc. (Jacksonville, FL) from 1990 to 1998: 3 510(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 Universal Technology Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Universal Technology Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Universal Technology Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?