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Physiodynamics, Inc.

Country not established

Devices
1

What Physiodynamics, Inc. makes

Physiodynamics, Inc. manufactures THERASTIM, a device designed for transcutaneous electrical nerve stimulation (TENS) therapy to manage chronic pain.

THERASTIM is classified as a Class II medical device in the US and is authorised via the FDA’s 510(k) pathway. The company 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

  • Therastim Ref K893851

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

Frequently asked questions

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

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

Which registries list Physiodynamics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Physiodynamics, Inc. include THERASTIM.

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