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Neumetry Medical, Inc.

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Devices
1

What Neumetry Medical, Inc. makes

Neumetry Medical, Inc. manufactures the SomnoMetry device, a medical system designed for respiratory monitoring and analysis during sleep studies.

The SomnoMetry system 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • SomnoMetry Ref K221179

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

Frequently asked questions

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

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

Which registries list Neumetry Medical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Neumetry Medical, Inc. include SomnoMetry.

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