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Kovision Mfg., Ltd.

ChinaFDA 510(k) applicant, unverified

Devices
1

What Kovision Mfg., Ltd. makes

Kovision Mfg., Ltd. manufactures eyewear and spectacles designed for vision correction and general use.

These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Eyewear/Spectacles Ref K945925

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Kovision Mfg., Ltd. have in the registry?

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

Which registries list Kovision Mfg., Ltd.'s devices?

Among its 1 most recently registered device, Kovision Mfg., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Kovision Mfg., Ltd.'s devices fall under?

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

What are the newest devices from Kovision Mfg., Ltd. in the registry?

The most recently registered devices listed for Kovision Mfg., Ltd. include EYEWEAR/SPECTACLES.

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