Col-Bar, Ltd.
Country not established
- Devices
- 1
What Col-Bar, Ltd. makes
Col-Bar, Ltd. makes the BIOBAR, an implantable biodegradable collagen membrane used for guided bone regeneration.
The BIOBAR is classified as a Class II medical device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Col-Bar, Ltd. have in the registry?
The registry currently lists 1 device for Col-Bar, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Col-Bar, Ltd.'s devices?
Among its 1 most recently registered device, Col-Bar, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Col-Bar, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Col-Bar, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Col-Bar, Ltd. in the registry?
The most recently registered devices listed for Col-Bar, Ltd. include BIOBAR, IMPLANTABLE BIODEGRADABLE COLLAGEN MEMBRANE FOR GUIDED BONE REGENERATION.