Vgi, LLC is one of 20175 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vgi, LLC - FDA 510(k) Cleared Devices
Recent clearances: VerteLP Interbody Fusion Device
1
Total
1
Cleared
0
Denied
Vgi, LLC has 1 FDA 510(k) cleared medical devices. Based in St. Petersburg, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Vgi, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Silver Pine Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vgi, LLC
1 devices