Applied Biomaterial Technologies
Country not established
- Devices
- 7
What Applied Biomaterial Technologies makes
Applied Biomaterial Technologies manufactures soft tissue implants and dural substitutes for reconstructive and cosmetic procedures, including nasal, chin, and breast implants, as well as dural sheeting for spinal applications.
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
The Nautilus Nasal Implant Ref K902283
Regimes: 510(k) Registry: 510(k)Pec Implant Ref K913768
Regimes: 510(k) Registry: 510(k)Zymalar Implant Ref K902284
Regimes: 510(k) Registry: 510(k)Duralastic Sheeting Ref K945552
Regimes: 510(k) Registry: 510(k)The Magnum Chin Implant Ref K902285
Regimes: 510(k) Registry: 510(k)The Permaridge Matrix Chin Ref K931500
Regimes: 510(k) Registry: 510(k)Duralastic Sheeting Ref K935571
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Applied Biomaterial Technologies have in the registry?
The registry currently lists 7 devices for Applied Biomaterial Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Biomaterial Technologies's devices?
Among its 7 most recently registered devices, Applied Biomaterial Technologies has devices listed in FDA 510(k) (7 devices).
What risk classes do Applied Biomaterial Technologies's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Applied Biomaterial Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Biomaterial Technologies in the registry?
The most recently registered devices listed for Applied Biomaterial Technologies include THE NAUTILUS NASAL IMPLANT, PEC IMPLANT, ZYMALAR IMPLANT and DURALASTIC SHEETING.