510(k) Report

FDA applicant

Stimulation Technology, Inc.

Mchenry, IL6 decisions1977–19790 recalls

FDA records 6 decisions for Stimulation Technology, Inc. (Mchenry, IL) from 1977 to 1979: 6 510(k) clearances. Most are in product codes GXY (Electrode, Cutaneous) 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, neurology panel, where it files most

How often FDA has decided Stimulation Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stimulation Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Stimulation Technology, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • GXYElectrode, Cutaneous3decisions
  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief2decisions
  • IPFStimulator, Muscle, Powered1decision

What has FDA decided for it lately?

  • K791048Stimtech Neuromuscular Stimulator, C 600Stimulation Technology, Inc. · 1979
  • K790345Stimtech Tens ElectrodeStimulation Technology, Inc. · 1979
  • K781565Electrical Nerve Stimulator Model 6035Stimulation Technology, Inc. · 1978
  • K772224Nerve Stimulator, Elec. TranscutaneousStimulation Technology, Inc. · 1977
  • K770447Epc InsticksStimulation Technology, Inc. · 1977
  • K770448Ins - T.E.N.S.Stimulation Technology, Inc. · 1977

All 6 as Stimulation Technology, Inc. →