Facetlink Dba Linkspine
Country not established
- Devices
- 2
What Facetlink Dba Linkspine makes
Facetlink Dba Linkspine manufactures spinal fusion platforms, including the CorticaLINK and VertebraLINK systems, designed for surgical interventions in the spine. These devices are intended for use in procedures requiring rigid fixation to promote bone fusion and structural stability.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the United States, where the manufacturer is based.
Catalogue
CorticaLINK Spinal Fusion Platform Ref K160722
510(k) 510(k)VertebraLINK Fusion Platform Ref K162693
510(k) 510(k)
Frequently asked questions
How many devices does Facetlink Dba Linkspine have in the registry?
The registry currently lists 2 devices for Facetlink Dba Linkspine. Devices recorded under merged duplicate company entries are counted once.
Which registries list Facetlink Dba Linkspine's devices?
Among its 2 most recently registered devices, Facetlink Dba Linkspine has devices listed in FDA 510(k) (2 devices).
What risk classes do Facetlink Dba Linkspine's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Facetlink Dba Linkspine's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Facetlink Dba Linkspine in the registry?
The most recently registered devices listed for Facetlink Dba Linkspine include CorticaLINK Spinal Fusion Platform and VertebraLINK Fusion Platform.