Altatec Biotechnologies
Country not established
- Devices
- 5
What Altatec Biotechnologies makes
Altatec Biotechnologies manufactures dental implant systems, including screw and cylinder implants for oral reconstruction, as well as ceramic abutments for implant-supported restorations.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Camlog Rootform Implant System Ref K000100
Regimes: 510(k) Registry: 510(k)Screwline Ref K022425
Regimes: 510(k) Registry: 510(k)Camlog Screw Implant System Ref K000099
Regimes: 510(k) Registry: 510(k)Altatec Ceramic Abutment Ref K032448
Regimes: 510(k) Registry: 510(k)Camlog Cylinder Implant System Ref K000065
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Altatec Biotechnologies have in the registry?
The registry currently lists 5 devices for Altatec Biotechnologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Altatec Biotechnologies's devices?
Among its 5 most recently registered devices, Altatec Biotechnologies has devices listed in FDA 510(k) (5 devices).
What risk classes do Altatec Biotechnologies's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Altatec Biotechnologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Altatec Biotechnologies in the registry?
The most recently registered devices listed for Altatec Biotechnologies include CAMLOG ROOTFORM IMPLANT SYSTEM, SCREWLINE, CAMLOG SCREW IMPLANT SYSTEM and ALTATEC CERAMIC ABUTMENT.