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Vasogenics, Inc.

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Devices
1

What Vasogenics, Inc. makes

Vasogenics, Inc. manufactures the EECP-MC2, a device used for external counterpulsation therapy to improve blood flow and support cardiac function in patients with certain heart conditions.

The EECP-MC2 is classified as a Class II medical device and is listed under the FDA’s 510(k) clearance process. 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

  • Vasogenics Eecp-MC2 Ref K940264

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

Frequently asked questions

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

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

Which registries list Vasogenics, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Vasogenics, Inc. include VASOGENICS EECP-MC2.

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