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Hurricane Hardware, Inc.

TaiwanFDA applicant, unverified

Devices
1

What Hurricane Hardware, Inc. makes

Hurricane Hardware, Inc. makes the HURRICANE device.

The HURRICANE device is classified as Class I and is listed in the FDA 510(k) registry. 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

  • Hurricane Ref K952258

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

Frequently asked questions

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

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

Which registries list Hurricane Hardware, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Hurricane Hardware, Inc. include HURRICANE.

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