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Medwand Solutions, Inc.

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Devices
1

What Medwand Solutions, Inc. makes

Medwand Solutions, Inc. manufactures the MedWand, a handheld ultrasound device designed for point-of-care imaging, enabling real-time visualization of internal structures for diagnostic purposes.

The MedWand is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • MedWand Ref K212975

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

Frequently asked questions

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

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

Which registries list Medwand Solutions, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Medwand Solutions, Inc. include MedWand.

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