Medical Device Manufacturer · US , St. Petersburg , FL

Vgi, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Recent clearances: VerteLP Interbody Fusion Device

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Vgi, LLC Orthopedic ✕

1 devices

1-1 of 1

Cleared Jan 13, 2016

VerteLP Interbody Fusion Device

Orthopedic · 240d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 22, 2026