Co-Ligne AG
Country not established
- Devices
- 695
What Co-Ligne AG makes
Co-Ligne AG makes spinal fixation systems, including the GII SPINAL FIXATION SYSTEM and the OSTAPEK VBR SYSTEM, which include components such as axial screws. These products are types of medical devices used in spinal procedures.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
Search and filter all 695 devicesShowing 1-50 of 695
Frequently asked questions
How many devices does Co-Ligne AG have in the registry?
The registry currently lists 695 devices for Co-Ligne AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Co-Ligne AG's devices?
Among its 50 most recently registered devices, Co-Ligne AG has devices listed in FDA GUDID (50 devices).
What risk classes do Co-Ligne AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Co-Ligne AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Co-Ligne AG in the registry?
The most recently registered devices listed for Co-Ligne AG include Trabis® 015.030.251, VBR 65.712, VBR 2369 and ostaPek Interbody Fusion Cage 66.335.