Oct, USA, Inc.
Country not established
- Devices
- 1
What Oct, USA, Inc. makes
Oct, USA, Inc. manufactures bone substitutes classified as BBP (bone void fillers and bone substitution products) designed for orthopedic applications, including bone defect filling and structural support in surgical procedures.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Bbp Bone Substitutes Ref K030195
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oct, USA, Inc. have in the registry?
The registry currently lists 1 device for Oct, USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oct, USA, Inc.'s devices?
Among its 1 most recently registered device, Oct, USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oct, USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oct, USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oct, USA, Inc. in the registry?
The most recently registered devices listed for Oct, USA, Inc. include BBP BONE SUBSTITUTES.