# Hyprevention Sas

- Location (FDA's records): Pessac Cedex, FR
- FDA decisions: 2 (2020–2024): 2 510(k) clearances
- Names in FDA's records: Hyprevention Sas (1); Hyprevention (1)
- Product codes: NDN (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 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
- Benvenue Medical, Inc.: 1 (https://510kreport.com/company/benvenue-medical)

## Firms that cite its devices most
- Slk Ortho, LLC: 1 (https://510kreport.com/company/slk-ortho)

## Its most-cited devices
- K191709: V-STRUT Vertebral Implant (2020), cited by 2

## Recent decisions
- K240084: V-STRUT® Vertebral Implant (Feb 9, 2024)
- K191709: V-STRUT Vertebral Implant (Mar 5, 2020)

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