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Frindley Enterprise Co., Ltd.

TaiwanFDA applicant, unverified

Devices
1

What Frindley Enterprise Co., Ltd. makes

Frindley Enterprise Co., Ltd. makes the Frindley Enterprise Co device.

This 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

  • Frindley Enterprise Co Ref K942142

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

Frequently asked questions

How many devices does Frindley Enterprise Co., Ltd. have in the registry?

The registry currently lists 1 device for Frindley Enterprise Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Frindley Enterprise Co., Ltd.'s devices?

Among its 1 most recently registered device, Frindley Enterprise Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Frindley Enterprise Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Frindley Enterprise Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Frindley Enterprise Co., Ltd. in the registry?

The most recently registered devices listed for Frindley Enterprise Co., Ltd. include FRINDLEY ENTERPRISE CO.

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