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Mt. Hood Mfr., Inc.

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Devices
1

What Mt. Hood Mfr., Inc. makes

Mt. Hood Mfr., Inc. makes medical devices such as the SUNMASTER, which falls under the category of Class II devices.

The company's portfolio is regulated and listed in the fda_510k registry, and it is based in the US.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Sunmaster Ref K842276

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

Frequently asked questions

How many devices does Mt. Hood Mfr., Inc. have in the registry?

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

Which registries list Mt. Hood Mfr., Inc.'s devices?

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

What risk classes do Mt. Hood Mfr., Inc.'s devices fall under?

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

What are the newest devices from Mt. Hood Mfr., Inc. in the registry?

The most recently registered devices listed for Mt. Hood Mfr., Inc. include SUNMASTER.

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