Lifelink Foundation Tissue Bank
Country not established
- Devices
- 1
What Lifelink Foundation Tissue Bank makes
Lifelink Foundation Tissue Bank provides human-derived dura mater grafts, used in neurosurgical and spinal procedures to repair or replace damaged dura layers.
The dura mater grafts are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company operates within the United States.
Catalogue
Dura Mater Ref K910447
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifelink Foundation Tissue Bank have in the registry?
The registry currently lists 1 device for Lifelink Foundation Tissue Bank. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifelink Foundation Tissue Bank's devices?
Among its 1 most recently registered device, Lifelink Foundation Tissue Bank has devices listed in FDA 510(k) (1 device).
What risk classes do Lifelink Foundation Tissue Bank's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lifelink Foundation Tissue Bank's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifelink Foundation Tissue Bank in the registry?
The most recently registered devices listed for Lifelink Foundation Tissue Bank include DURA MATER.