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Neo Group Limited

Hong Kong SAR ChinaFDA applicant, unverified

Devices
1

What Neo Group Limited makes

Neo Group Limited manufactures dental zirconia restorations, including the NEO DENTA ZIRCONIA, which are used for crowns, bridges, and other fixed dental prosthetics.

The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. Neo Group Limited 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

  • Neo Denta Zirconia Ref K130198

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

Frequently asked questions

How many devices does Neo Group Limited have in the registry?

The registry currently lists 1 device for Neo Group Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list Neo Group Limited's devices?

Among its 1 most recently registered device, Neo Group Limited has devices listed in FDA 510(k) (1 device).

What risk classes do Neo Group Limited's devices fall under?

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

What are the newest devices from Neo Group Limited in the registry?

The most recently registered devices listed for Neo Group Limited include NEO DENTA ZIRCONIA.

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