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Jyoti Ceramic Industries Private Limited

IndiaFDA 510(k) applicant, unverified

Devices
1

What Jyoti Ceramic Industries Private Limited makes

Jyoti Ceramic Industries Private Limited manufactures dental ceramic blocks and discs designed for computer-aided design/computer-aided manufacturing (CAD/CAM) systems, including the ZIECON DISC WITH COLLAR (ZD810-26) and ZIECON BLOCK variants (e.g., ZB763812-20, ZB653012-21, ZB402012-20). These products are intended for dental restorations, such as crowns and bridges, and are compatible with milling machines for precision fabrication.

The company’s portfolio is classified under Class II medical devices in the US and is subject to 510(k) premarket notification requirements through the FDA. The devices are listed under the FDA’s 510(k) registry, and the manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Frequently asked questions

How many devices does Jyoti Ceramic Industries Private Limited have in the registry?

The registry currently lists 1 device for Jyoti Ceramic Industries Private Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list Jyoti Ceramic Industries Private Limited's devices?

Among its 1 most recently registered device, Jyoti Ceramic Industries Private Limited has devices listed in FDA 510(k) (1 device).

What risk classes do Jyoti Ceramic Industries Private Limited's devices fall under?

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

What are the newest devices from Jyoti Ceramic Industries Private Limited in the registry?

The most recently registered devices listed for Jyoti Ceramic Industries Private Limited include ZIECON DISC WITH COLLAR FOR CAD/CAM MODEL ZD810-26, ZIECON BLOCK FOR MOM MODEL ZB763812-20, ZB653012-21, ZB402012-20, ZI.

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