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Creodent Prosthetics Ltd

United Statesfrom the FDA registration address FDA establishment FEI 3009711592

Devices
9
Registrations
FDA
FDA recalls
0

What Creodent Prosthetics Ltd makes

Creodent Prosthetics Ltd manufactures custom dental abutments and orthodontic aligners, including the CreoDent Solidex Custom Abutment and related screw assemblies, as well as the Creokorrekt Aligners product line.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Company details

FDA FEI number
3009711592
Address
29 W 30th St FL 11th, New York, NY, 10001

Frequently asked questions

How many devices does CREODENT PROSTHETICS LTD have in the registry?

The registry currently lists 9 devices for CREODENT PROSTHETICS LTD. Devices recorded under merged duplicate company entries are counted once.

Which registries list CREODENT PROSTHETICS LTD's devices?

Among its 9 most recently registered devices, CREODENT PROSTHETICS LTD has devices listed in FDA 510(k) (9 devices).

What risk classes do CREODENT PROSTHETICS LTD's devices fall under?

Among its 9 most recently registered devices, the classes recorded for CREODENT PROSTHETICS LTD's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from CREODENT PROSTHETICS LTD in the registry?

The most recently registered devices listed for CREODENT PROSTHETICS LTD include CREODENT SOLIDEX CUSTOM ABUTMENT, CreoDent Solidex Customized Abutment, CREOKORREKT Aligners and CreoDent Solidex Customized Abutment and Screw.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.