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Medicus Technologies, Inc.

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Devices
1

What Medicus Technologies, Inc. makes

Medicus Technologies, Inc. manufactures the SICKLE-2000, a medical device designed for the treatment or management of sickle cell disease, likely involving mechanical or therapeutic interventions for blood flow or oxygenation.

The SICKLE-2000 is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. 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

  • Sickle-2000 Ref K955719

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

Frequently asked questions

How many devices does Medicus Technologies, Inc. have in the registry?

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

Which registries list Medicus Technologies, Inc.'s devices?

Among its 1 most recently registered device, Medicus Technologies, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Medicus Technologies, Inc.'s devices fall under?

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

What are the newest devices from Medicus Technologies, Inc. in the registry?

The most recently registered devices listed for Medicus Technologies, Inc. include SICKLE-2000.

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