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Dentaim Co., Ltd.

South KoreaFDA applicant, unverified

Devices
1

What Dentaim Co., Ltd. makes

Dentaim Co., Ltd. manufactures the ZMATCH BLOCK, a dental device designed for orthodontic treatment to aid in tooth alignment and bite correction.

The ZMATCH BLOCK is classified as a Class II medical device and is listed under the FDA’s 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

  • Zmatch Block Ref K083201

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

Frequently asked questions

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

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

Which registries list Dentaim Co., Ltd.'s devices?

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

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

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

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

The most recently registered devices listed for Dentaim Co., Ltd. include ZMATCH BLOCK.

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