# Vgi, LLC

- Location (FDA's records): St. Petersburg, FL
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: OVD (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Ldr Spine USA: 1 (https://510kreport.com/company/ldr-spine-usa)
- Globus Medical, Inc.: 1 (https://510kreport.com/company/globus-medical)

## Recent decisions
- K151312: VerteLP Interbody Fusion Device (Jan 13, 2016)

Source page: https://510kreport.com/company/vgi