Advanced Biomaterials
Country not established
- Devices
- 3
What Advanced Biomaterials makes
Advanced Biomaterials manufactures orthopedic fixation devices, including cannulated interference screws made from polylactic acid (PLLA), titanium, and a composite material designed for absorbable fixation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Plla Cannulated Interference Screw Ref K032830
510(k) 510(k)Titanium Cannulated Interference Screw Ref K033749
510(k) 510(k)Triabsorb Composite Screw Ref K050468
510(k) 510(k)
Frequently asked questions
How many devices does Advanced Biomaterials have in the registry?
The registry currently lists 3 devices for Advanced Biomaterials. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Biomaterials's devices?
Among its 3 most recently registered devices, Advanced Biomaterials has devices listed in FDA 510(k) (3 devices).
What risk classes do Advanced Biomaterials's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Advanced Biomaterials's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advanced Biomaterials in the registry?
The most recently registered devices listed for Advanced Biomaterials include PLLA CANNULATED INTERFERENCE SCREW, TITANIUM CANNULATED INTERFERENCE SCREW and TRIABSORB COMPOSITE SCREW.