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Theri-Teck, Inc.

Country not established

Devices
1

What Theri-Teck, Inc. makes

Theri-Teck, Inc. manufactures the MICRO-STIM 200, a device designed for neuromuscular electrical stimulation, used in physical therapy and rehabilitation settings to stimulate muscle contractions and improve function.

The MICRO-STIM 200 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

  • Micro-Stim 200 Ref K885190

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

Frequently asked questions

How many devices does Theri-Teck, Inc. have in the registry?

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

Which registries list Theri-Teck, Inc.'s devices?

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

What risk classes do Theri-Teck, Inc.'s devices fall under?

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

What are the newest devices from Theri-Teck, Inc. in the registry?

The most recently registered devices listed for Theri-Teck, Inc. include MICRO-STIM 200.

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