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Seo Han Corp., Ltd.

South KoreaFDA applicant, unverified

Devices
1

What Seo Han Corp., Ltd. makes

Seo Han Corp., Ltd. manufactures spectacle frames, which are designed for use in eyeglasses and corrective eyewear.

The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer 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

  • Spectacle Frame Ref K945392

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

Frequently asked questions

How many devices does Seo Han Corp., Ltd. have in the registry?

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

Which registries list Seo Han Corp., Ltd.'s devices?

Among its 1 most recently registered device, Seo Han Corp., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Seo Han Corp., Ltd.'s devices fall under?

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

What are the newest devices from Seo Han Corp., Ltd. in the registry?

The most recently registered devices listed for Seo Han Corp., Ltd. include SPECTACLE FRAME.

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