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Deepvoxel, Inc.

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Devices
1

What Deepvoxel, Inc. makes

Deepvoxel, Inc. manufactures the DV. Target, a medical imaging device designed for targeted visualization and analysis in radiology applications, likely supporting diagnostic or treatment planning workflows.

The DV. Target is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • DV. Target Ref K202928

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

Frequently asked questions

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

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

Which registries list Deepvoxel, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Deepvoxel, Inc. include DV. Target.

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