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Oriental Resources Development Limited Biomedical Factory

Country not established

Devices
2

What Oriental Resources Development Limited Biomedical Factory makes

The company produces synthetic bone graft substitutes designed for use in orthopedic and reconstructive surgeries. These products are intended to replace or augment bone tissue, supporting healing in procedures such as spinal fusion, fracture repair, and defect reconstruction.

The portfolio consists of Class II medical devices, regulated under the FDA’s Unique Device Identifier (UDI) system. These products are listed in the FDA’s UDI database, ensuring traceability and compliance with U.S. regulatory requirements.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Company details

DUNS number
658871135

Frequently asked questions

How many devices does ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY have in the registry?

The registry currently lists 2 devices for ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY. Devices recorded under merged duplicate company entries are counted once.

Which registries list ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY's devices?

Among its 2 most recently registered devices, ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY has devices listed in FDA GUDID (2 devices).

What risk classes do ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY's devices fall under?

Among its 2 most recently registered devices, the classes recorded for ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY in the registry?

The most recently registered devices listed for ORIENTAL RESOURCES DEVELOPMENT LIMITED BIOMEDICAL FACTORY include NuROs Bone Graft Substitute(Sterile) BGD50 and NuROs Bone Graft Substitute(Sterile) NBP50.

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