Vgi, LLC
Country not established
- Devices
- 1
What Vgi, LLC makes
Vgi, LLC manufactures the VerteLP Interbody Fusion Device, a spinal implant designed for interbody fusion procedures in the lumbar spine.
The VerteLP Interbody Fusion Device is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
VerteLP Interbody Fusion Device Ref K151312
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vgi, LLC have in the registry?
The registry currently lists 1 device for Vgi, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vgi, LLC's devices?
Among its 1 most recently registered device, Vgi, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Vgi, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Vgi, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vgi, LLC in the registry?
The most recently registered devices listed for Vgi, LLC include VerteLP Interbody Fusion Device.