# Progentix Orthobiology BV

- Location (FDA's records): Bilthoven, NL
- FDA decisions: 2 (2009–2015): 2 510(k) clearances
- Product codes: MQV (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 8 (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
- Orthovita, Inc.: 1 (https://510kreport.com/company/orthovita)
- Isotis NV: 1 (https://510kreport.com/company/isotis)
- Apatech, Ltd.: 1 (https://510kreport.com/company/apatech)

## Firms that cite its devices most
- Nu Vasive, Incorporated: 4 (https://510kreport.com/company/nu-vasive)
- Zimmer Biomet Spine, Inc.: 1 (https://510kreport.com/company/zimmer-biomet-spine)
- Kuros Biosciences B.V: 1 (https://510kreport.com/company/kuros-biosciences-b-v)
- Xpand Biotechnology BV: 1 (https://510kreport.com/company/xpand-biotechnology)

## Its most-cited devices
- K090641: Curios (2009), cited by 4
- K151584: AttraX Putty (2015), cited by 4

## Recent decisions
- K151584: AttraX Putty (Oct 8, 2015)
- K090641: Curios (Oct 23, 2009)

Source page: https://510kreport.com/company/progentix-orthobiology