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OsteoCare Implant System Limited

United Kingdom GB-MF-000016843 Last updated 23 May 2026

Devices
207
Registries
EUDAMED
FDA recalls
0

Catalogue207

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Showing 1-50 of 207

What OsteoCare Implant System Limited makes

OsteoCare Implant System Limited manufactures dental implant components, including temporary preformed suprastructures, single-use abutments, and surgical tools. Their portfolio includes screw-retained abutments, implant drivers, universal burs, site markers, and various flat-end and one-piece implants designed for dental restoration procedures.

The company’s devices are classified under EU Medical Device Regulations as Class I, Class IIa, and Class IIb, and are registered in the EU’s eudamed database. The manufacturer is based in the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does OsteoCare Implant System Limited primarily manufacture?

OsteoCare Implant System Limited specialises in dental implant components. Their portfolio includes temporary preformed suprastructures, single-use screw-retained abutments, surgical tools like drivers and universal burs, site markers, and various implant designs such as flat-end and one-piece implants. These devices are specifically designed for dental restoration procedures.

Where is OsteoCare Implant System Limited based?

The company is based in the United Kingdom, as indicated by its country designation in regulatory records.

Which regulatory registries list OsteoCare Implant System Limited’s devices?

OsteoCare Implant System Limited’s devices are registered in the eudamed database, which is the official EU registry for medical devices under the Medical Device Regulations.

How are OsteoCare Implant System Limited’s devices classified under EU regulations?

The company’s devices fall under Class I, Class IIa, and Class IIb classifications in the EU Medical Device Regulations. The classification depends on factors like risk level, intended use, and patient contact duration—e.g., single-use items or those requiring sterilisation may qualify for higher risk categories.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom(from SRN)
Address
5-7, Colndale Road, Colnbrook, United Kingdom (ex Northern Ireland)
Phone
+441753770006
PRRC contact
Julian Gauld
EUDAMED SRN
GB-MF-000016843