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Xenos Medical Systems, Inc.

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Devices
1

What Xenos Medical Systems, Inc. makes

Xenos Medical Systems, Inc. makes the XENOS MOBILECAM, a medical imaging device designed for mobile use in clinical settings.

The XENOS MOBILECAM is classified as a Class I device and is listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Xenos Mobilecam Ref K893379

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

Frequently asked questions

How many devices does Xenos Medical Systems, Inc. have in the registry?

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

Which registries list Xenos Medical Systems, Inc.'s devices?

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

What risk classes do Xenos Medical Systems, Inc.'s devices fall under?

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

What are the newest devices from Xenos Medical Systems, Inc. in the registry?

The most recently registered devices listed for Xenos Medical Systems, Inc. include XENOS MOBILECAM.

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