510(k) Report

FDA applicant

Stimtech Products

Southbridge, MA3 decisions1989–19930 recalls

FDA records 3 decisions for Stimtech Products (Southbridge, MA) from 1989 to 1993: 3 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Stimtech Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stimtech Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • IPFStimulator, Muscle, Powered1decision
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision
  • KPIStimulator, Electrical, Non-Implantable, For Incontinence1decision

What has FDA decided for it lately?

  • K922562Stimtech PFX, Catalog Number 78-8540Stimtech Products · 1993
  • K903128Stimtrac PC, Catalog NO. 78-8510Stimtech Products · 1991
  • K895671Stimtrac II Catalog Number 78-8500Stimtech Products · 1989

All 3 as Stimtech Products →