# Ventris Medical

- Location (FDA's records): Newport Beach, CA
- FDA decisions: 5 (2022–2026): 5 510(k) clearances
- Product codes: MQV (4), KGN (1)
- 510(k) review time since 2016: median 88 days, against 57 for FDA's reviews in the same codes and years (4 of 5 faster)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Nu Vasive, Incorporated: 2 (https://510kreport.com/company/nu-vasive)
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Biostructures, LLC: 1 (https://510kreport.com/company/biostructures)
- Strukmyer Medical, LLC: 1 (https://510kreport.com/company/strukmyer-medical)

## Firms that cite its devices most
- SurGenTec, LLC: 1 (https://510kreport.com/company/surgentec)

## Its most-cited devices
- K240458: Synthetic Bone Putty (2024), cited by 1

## Recent decisions
- K260596: Collagen Wound Powder (Jul 2, 2026)
- K250556: Porous Biologic Scaffold (Mar 21, 2025)
- K240765: Porous Biologic Scaffold (Dec 18, 2024)
- K240458: Synthetic Bone Putty (Mar 7, 2024)
- K221644: Synthetic Bone Putty (Sep 2, 2022)

Source page: https://510kreport.com/company/ventris-medical