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Ov World Co., Ltd.

South KoreaFDA 510(k) applicant, unverified

Devices
1

What Ov World Co., Ltd. makes

Ov World Co., Ltd. manufactures the Omega VL, a Class II medical device designed for [specific application not provided in data]. This product is intended for [purpose not specified in data], adhering to regulatory standards for its category.

The Omega VL is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Omega VL Ref K162366

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Ov World Co., Ltd. have in the registry?

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

Which registries list Ov World Co., Ltd.'s devices?

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

What risk classes do Ov World Co., Ltd.'s devices fall under?

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

What are the newest devices from Ov World Co., Ltd. in the registry?

The most recently registered devices listed for Ov World Co., Ltd. include Omega VL.

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