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Stimulation Technology, Inc.

United StatesFDA applicant, unverified

Devices
6

What Stimulation Technology, Inc. makes

Stimulation Technology, Inc. manufactures transcutaneous electrical nerve stimulators (TENS) and neuromuscular stimulators, including disposable electrodes and portable devices for pain relief and muscle stimulation. Their products include models like the ELECTRICAL NERVE STIMULATOR MODEL 6035 and the STIMTECH NEUROMUSCULAR STIMULATOR C 600, as well as adhesive electrodes such as EPC INSTICKS and STIMTECH TENS ELECTRODES. These devices are designed for non-invasive therapeutic applications, including transcutaneous electrical nerve stimulation (TENS) and intermittent nerve stimulation (INS-T.E.N.S.).

The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. Their products are intended for use in the United States, where compliance with FDA requirements ensures their authorised market presence. No other regulatory registries or jurisdictions are specified.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

  • Nerve Stimulator, Elec. Transcutaneous Ref K772224

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Electrical Nerve Stimulator Model 6035 Ref K781565

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Epc Insticks Ref K770447

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Stimtech Neuromuscular Stimulator, C 600 Ref K791048

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Stimtech Tens Electrode Ref K790345

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ins - T.E.N.S. Ref K770448

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Stimulation Technology, Inc. have in the registry?

The registry currently lists 6 devices for Stimulation Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Stimulation Technology, Inc.'s devices?

Among its 6 most recently registered devices, Stimulation Technology, Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Stimulation Technology, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Stimulation Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Stimulation Technology, Inc. in the registry?

The most recently registered devices listed for Stimulation Technology, Inc. include NERVE STIMULATOR, ELEC. TRANSCUTANEOUS, ELECTRICAL NERVE STIMULATOR MODEL 6035, EPC INSTICKS and STIMTECH NEUROMUSCULAR STIMULATOR, C 600.

Generated automatically from registry data and not verified by a human reviewer.