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Myo-Tone, Inc.

Country not established

Devices
1

What Myo-Tone, Inc. makes

Myo-Tone, Inc. manufactures the SYSTEM-80, a device designed for neuromuscular stimulation and rehabilitation, likely targeting muscle strengthening or recovery applications.

The SYSTEM-80 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Myo-Tone, Inc. System-80 Ref K822250

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

Frequently asked questions

How many devices does Myo-Tone, Inc. have in the registry?

The registry currently lists 1 device for Myo-Tone, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Myo-Tone, Inc.'s devices?

Among its 1 most recently registered device, Myo-Tone, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Myo-Tone, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Myo-Tone, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Myo-Tone, Inc. in the registry?

The most recently registered devices listed for Myo-Tone, Inc. include MYO-TONE, INC. SYSTEM-80.

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