Full Golden Biotech Co., Ltd.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 2
What Full Golden Biotech Co., Ltd. makes
Full Golden Biotech Co., Ltd. manufactures FG Bone Graft M, a bone graft material designed for surgical applications in orthopedic and maxillofacial procedures.
The company’s portfolio is regulated under FDA’s Class II device classification, with FG Bone Graft M listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
FG Bone Graft B Ref K243745
510(k) 510(k)FG Bone Graft M Ref K244006
510(k) 510(k)
Frequently asked questions
How many devices does Full Golden Biotech Co., Ltd. have in the registry?
The registry currently lists 2 devices for Full Golden Biotech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Full Golden Biotech Co., Ltd.'s devices?
Among its 2 most recently registered devices, Full Golden Biotech Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Full Golden Biotech Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Full Golden Biotech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Full Golden Biotech Co., Ltd. in the registry?
The most recently registered devices listed for Full Golden Biotech Co., Ltd. include FG Bone Graft B and FG Bone Graft M.