Skip to content

Precision Electronics, Ltd.

Country not established

Devices
1

What Precision Electronics, Ltd. makes

Precision Electronics, Ltd. manufactures THERASTIM, a medical device designed for therapeutic stimulation applications.

THERASTIM is classified as a Class II device under FDA regulations and is listed via the 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

  • Therastim Ref K914813

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

Frequently asked questions

How many devices does Precision Electronics, Ltd. have in the registry?

The registry currently lists 1 device for Precision Electronics, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Precision Electronics, Ltd.'s devices?

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

What risk classes do Precision Electronics, Ltd.'s devices fall under?

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

What are the newest devices from Precision Electronics, Ltd. in the registry?

The most recently registered devices listed for Precision Electronics, Ltd. include THERASTIM.

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