# Ossacur AG

- Location (FDA's records): Santa Barbara, CA
- FDA decisions: 4 (2004–2006): 4 510(k) clearances
- Product codes: MQV (3), LYC (1)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 5 (3 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
- Curasan AG: 3 (https://510kreport.com/company/curasan)
- Regeneration Technologies, Inc.: 2 (https://510kreport.com/company/regeneration-technologies)
- Orquest, Inc.: 1 (https://510kreport.com/company/orquest)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Interpore Cross Intl.: 1 (https://510kreport.com/company/interpore-cross-intl)
- Curasan Ag, Frankfurt Facility: 1 (https://510kreport.com/company/curasan-ag-frankfurt-facility)

## Firms that cite its devices most
- Teknimed, S.A.: 1 (https://510kreport.com/company/teknimed)
- Kyung Won Medical Co., Ltd.: 1 (https://510kreport.com/company/kyung-won-medical)

## Its most-cited devices
- K053374: Ossaplast Dental (Particle Size of 500 to 1000 UM to 2000 UM) (2006), cited by 2
- K042305: Ossaplast Ortho, O.5ML, Model# 221 900, Ossaplast Ortho, 1.0ML, Model# 221 901, Ossaplast Ortho, 3.0ML, Model# 221 903 (2004), cited by 2
- K050416: Ossaplast Ortho (2005), cited by 1

## Recent decisions
- K051047: Colloss E Bone Void Filler (Mar 8, 2006)
- K053374: Ossaplast Dental (Particle Size of 500 to 1000 UM to 2000 UM) (Feb 21, 2006)
- K050416: Ossaplast Ortho (Mar 29, 2005)
- K042305: Ossaplast Ortho, O.5ML, Model# 221 900, Ossaplast Ortho, 1.0ML, Model# 221 901, Ossaplast Ortho, 3.0ML, Model# 221 903 (Oct 21, 2004)

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