# Biogeneration

- Location (FDA's records): Lakeland, TN
- FDA decisions: 2 (1998–2003): 2 510(k) clearances
- Product codes: MQV (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (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 that cite its devices most
- Nexa Orthopedics, Inc.: 2 (https://510kreport.com/company/nexa-orthopedics)

## Its most-cited devices
- K973704: Profusion Bone Void Filler (1998), cited by 1
- K031838: Profusion Bone Void Filler Kit (2003), cited by 1

## Recent decisions
- K031838: Profusion Bone Void Filler Kit (Oct 30, 2003)
- K973704: Profusion Bone Void Filler (Apr 3, 1998)

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