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Nemectron Medical, Inc.

United StatesFDA applicant, unverified

Devices
13

What Nemectron Medical, Inc. makes

Nemectron Medical, Inc. manufactures a range of electrotherapy and neuromuscular stimulation devices, including high-voltage pulsed therapy systems (e.g., NEMECTRODYN series), microwave therapy units (e.g., NEMECTRON MICROWAVE), and muscle stimulation devices (e.g., ENDOVAC 2 POWER MUSCLE STIM.). The portfolio also includes biofeedback tools like the EMG BIOFEEDBACK DEVICE, as well as thermal and pulsed energy devices such as THERMODYN and THERMOPULS E. Some products are designed for wound care, tissue stimulation, or rehabilitation applications.

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. These products are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States. The manufacturer is based in the US.

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

Catalogue13

Newest first, rows 1-13 of 13

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  • Nemectrodyn 8 Ref K802804

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

  • Nemdi Ref K843734

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

  • Thermopuls E Ref K844416

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

  • Softepil Ref K843735

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

  • Nemectron Microwave Ref K895000

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

  • Nemectrodyn Model 2 & Endovac 2 Ref K854721

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

  • Nemectrodyn Models 8, 7, 5 (Vols. I-Iv Ref K820334

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

  • Thermodyn Ref K923396

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

  • Nemectrodyn Model 2 & Endovac 2 Power Muscle Stim. Ref K854720

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

  • Nemectroson Model 2 Ref K862376

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

  • Nemectrodyn 5 Ref K802805

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

  • Emg Biofeedback Device Ref K823511

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

  • Electrodyn Cii-Interferential Muscle Ref K810513

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

Rows 1-13 of 13

Frequently asked questions

How many devices does Nemectron Medical, Inc. have in the registry?

The registry currently lists 13 devices for Nemectron Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nemectron Medical, Inc.'s devices?

Among its 13 most recently registered devices, Nemectron Medical, Inc. has devices listed in FDA 510(k) (13 devices).

What risk classes do Nemectron Medical, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Nemectron Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Nemectron Medical, Inc. in the registry?

The most recently registered devices listed for Nemectron Medical, Inc. include NEMECTRODYN 8, NEMDI, THERMOPULS E and SOFTEPIL.

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