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Korea Engineering Plastics Co., Ltd.

South KoreaFDA 510(k) applicant, unverified

Devices
1

What Korea Engineering Plastics Co., Ltd. makes

Korea Engineering Plastics Co., Ltd. manufactures denture base resin. This product is a specialized material used in the fabrication of dental prosthetics.

The company is based in the US and maintains products that are classified as Class II medical devices. These devices are listed within the FDA 510(k) regulatory registry.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Denture base resin Ref K152270

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

Frequently asked questions

How many devices does Korea Engineering Plastics Co., Ltd. have in the registry?

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

Which registries list Korea Engineering Plastics Co., Ltd.'s devices?

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

What risk classes do Korea Engineering Plastics Co., Ltd.'s devices fall under?

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

What are the newest devices from Korea Engineering Plastics Co., Ltd. in the registry?

The most recently registered devices listed for Korea Engineering Plastics Co., Ltd. include Denture base resin.

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