FDA applicant

Th Charters, Inc.

Beaverton, OR8 decisions1980–19870 recalls

FDA records 8 decisions for Th Charters, Inc. (Beaverton, OR) from 1980 to 1987: 8 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and 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 Th Charters, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Th Charters, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Th Charters, Inc.

Which product codes does it file in?

What has FDA decided for it lately?