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Enertron Engineering Co.

TaiwanFDA applicant, unverified

Devices
1

What Enertron Engineering Co. makes

Enertron Engineering Co. manufactures the ENERTRON CPR Jack, a device designed to assist in cardiopulmonary resuscitation (CPR) procedures by providing a stable platform for chest compressions.

The ENERTRON CPR Jack is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance 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

  • Enertron Cpr Jack Ref K024215

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

Frequently asked questions

How many devices does Enertron Engineering Co. have in the registry?

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

Which registries list Enertron Engineering Co.'s devices?

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

What risk classes do Enertron Engineering Co.'s devices fall under?

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

What are the newest devices from Enertron Engineering Co. in the registry?

The most recently registered devices listed for Enertron Engineering Co. include ENERTRON CPR JACK.

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