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Fujisawa Electronics Co.

Country not established

Devices
1

What Fujisawa Electronics Co. makes

Fujisawa Electronics Co. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the TENS MAX model, designed for pain management through electrical stimulation.

The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Tens Max Ref K823388

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Fujisawa Electronics Co. have in the registry?

The registry currently lists 1 device for Fujisawa Electronics Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Fujisawa Electronics Co.'s devices?

Among its 1 most recently registered device, Fujisawa Electronics Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Fujisawa Electronics Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Fujisawa Electronics Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Fujisawa Electronics Co. in the registry?

The most recently registered devices listed for Fujisawa Electronics Co. include TENS MAX.

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