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Oxycheck, Inc.

Country not established

Devices
1

What Oxycheck, Inc. makes

Oxycheck, Inc. manufactures the OXYCHECK OXYGEN MONITOR, a device designed to continuously monitor and display oxygen saturation levels in patients.

The OXYCHECK OXYGEN MONITOR is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. 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

  • Oxycheck Oxygen Monitor Ref K951038

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

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

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

Which registries list Oxycheck, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Oxycheck, Inc. include OXYCHECK OXYGEN MONITOR.

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