Center For Biomaterials and Advanced Technologies
Country not established
- Devices
- 1
What Center For Biomaterials and Advanced Technologies makes
The company produces reinforced absorbable synthetic surgical mesh, designed for use in hernia repair and soft tissue reinforcement procedures.
This product is classified as a Class II medical device under FDA regulations and is authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Reinforced Absorbable Synthetic Surgical Mesh Ref K023328
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Center For Biomaterials and Advanced Technologies have in the registry?
The registry currently lists 1 device for Center For Biomaterials and Advanced Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Center For Biomaterials and Advanced Technologies's devices?
Among its 1 most recently registered device, Center For Biomaterials and Advanced Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Center For Biomaterials and Advanced Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Center For Biomaterials and Advanced Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Center For Biomaterials and Advanced Technologies in the registry?
The most recently registered devices listed for Center For Biomaterials and Advanced Technologies include REINFORCED ABSORBABLE SYNTHETIC SURGICAL MESH.