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Cortecs, Ltd.

Country not established

Devices
1

What Cortecs, Ltd. makes

Cortecs, Ltd. manufactures the HELISAL RAPID BLOOD TEST, a diagnostic device designed for rapid blood analysis.

The HELISAL RAPID BLOOD TEST is classified as a Class I medical device and is listed under 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

  • Helisal Rapid Blood Test Ref K953686

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

Frequently asked questions

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

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

Which registries list Cortecs, Ltd.'s devices?

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

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

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

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

The most recently registered devices listed for Cortecs, Ltd. include HELISAL RAPID BLOOD TEST.

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