Osteopore, Inc.
Country not established
- Devices
- 1
What Osteopore, Inc. makes
Osteopore, Inc. manufactures the Osteopore PCL Scaffold, a biodegradable polymer-based structure designed to support bone regeneration and healing in orthopedic applications.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The scaffold is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Osteopore Pcl Scaffold Ref K051093
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osteopore, Inc. have in the registry?
The registry currently lists 1 device for Osteopore, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osteopore, Inc.'s devices?
Among its 1 most recently registered device, Osteopore, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Osteopore, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Osteopore, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osteopore, Inc. in the registry?
The most recently registered devices listed for Osteopore, Inc. include OSTEOPORE PCL SCAFFOLD.