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Arocep Enterprises, Ltd.

CanadaFDA applicant, unverified

Devices
1

What Arocep Enterprises, Ltd. makes

Arocep Enterprises, Ltd. makes medical devices such as the STRESS HANDLER.

The company's portfolio, which includes Class I devices, is listed in the FDA 510k registry, and Arocep Enterprises, Ltd. is based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Stress Handler Ref K936148

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

Frequently asked questions

How many devices does Arocep Enterprises, Ltd. have in the registry?

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

Which registries list Arocep Enterprises, Ltd.'s devices?

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

What risk classes do Arocep Enterprises, Ltd.'s devices fall under?

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

What are the newest devices from Arocep Enterprises, Ltd. in the registry?

The most recently registered devices listed for Arocep Enterprises, Ltd. include STRESS HANDLER.

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