# Aap Biomaterials GmbH & Co. KG

- Location (FDA's records): Dieburg, DE
- FDA decisions: 4 (2009–2013): 4 510(k) clearances
- Names in FDA's records: Aap Biomaterials GmbH & Co. KG (2); Aap Biomaterials GmbH (2)
- Product codes: LOD (2), NDN (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 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
- Heraeus Kulzer, Inc.: 3 (https://510kreport.com/company/heraeus-kulzer)
- Teknimed, S.A.: 1 (https://510kreport.com/company/teknimed)

## Firms that cite its devices most
- Osartis GmbH: 1 (https://510kreport.com/company/osartis)

## Its most-cited devices
- K090460: Bonos Inject (2009), cited by 2

## Recent decisions
- K123225: Bonos R 1X20, Bonos R 2X20, Bonos R 1X40, Bonos R 2X40, Bonos R 1X60 (Mar 15, 2013)
- K123081: Bonos R Genta 1X20 Model 01-0228; Bonos R Genta 2X20 Model 01-0229; Bonos R Genta 1X40 Model 01-0217; Bonos R Genta 2X40 (Mar 7, 2013)
- K121876: Vertecem II Cement Kit (Oct 19, 2012)
- K090460: Bonos Inject (Apr 14, 2009)

Source page: https://510kreport.com/company/aap-biomaterials