Oriental Resources Development Limited
TaiwanFDA 510(k) applicant, unverified FDA FEI 3010275504
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Oriental Resources Development Limited makes
Oriental Resources Development Limited manufactures the NUROS Bone Graft Substitute, a synthetic material designed to replace or augment bone tissue in surgical procedures.
The company’s portfolio is regulated under FDA’s Class II designation and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Nuros Bone Graft Substitute Ref K140913
510(k) 510(k)
Company details
- FDA FEI number
- 3010275504
- Address
- No.30, Hexing Rd.,, Hukou Township Hsinchu(County)
Frequently asked questions
How many devices does Oriental Resources Development Limited have in the registry?
The registry currently lists 1 device for Oriental Resources Development Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oriental Resources Development Limited's devices?
Among its 1 most recently registered device, Oriental Resources Development Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Oriental Resources Development Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oriental Resources Development Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oriental Resources Development Limited in the registry?
The most recently registered devices listed for Oriental Resources Development Limited include NUROS BONE GRAFT SUBSTITUTE.