Synoross Dba Osseone
Country not established
- Devices
- 2
What Synoross Dba Osseone makes
Synoross Dba Osseone makes the OsseOne Dental Implant System, a device used for dental implantation procedures.
The OsseOne Dental Implant System 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
OsseOne Dental Implant System Ref K182293
510(k) 510(k)OsseOne Dental Implant System Ref K233271
510(k) 510(k)
Frequently asked questions
How many devices does Synoross Dba Osseone have in the registry?
The registry currently lists 2 devices for Synoross Dba Osseone. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synoross Dba Osseone's devices?
Among its 2 most recently registered devices, Synoross Dba Osseone has devices listed in FDA 510(k) (2 devices).
What risk classes do Synoross Dba Osseone's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Synoross Dba Osseone's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Synoross Dba Osseone in the registry?
The most recently registered devices listed for Synoross Dba Osseone include OsseOne Dental Implant System.