# Medicrea

- Location (FDA's records): Round Rock, TX
- FDA decisions: 4 (2003–2010): 4 510(k) clearances
- Product codes: MQV (1), ODP (1), MNI (1), KWP (1)
- Predicates its devices cite: 11 (1 its own); citations of its devices by later devices: 6 (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
- Encore Orthopedics, Inc.: 6 (https://510kreport.com/company/encore-orthopedics)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)

## Firms that cite its devices most
- Medicrea International SA: 3 (https://510kreport.com/company/medicrea-international)
- Medicrea Technologies: 2 (https://510kreport.com/company/medicrea-technologies)

## Its most-cited devices
- K062136: Pass 2 Spinal System (2006), cited by 3
- K032094: Passmed Spinal System (2003), cited by 3

## Recent decisions
- K100484: Impix Manta Cervical Interbody Device (Mar 16, 2010)
- K062136: Pass 2 Spinal System (Oct 6, 2006)
- K050490: Osmosys Calcium Phosphate Ceramic Bone Filler (Apr 11, 2005)
- K032094: Passmed Spinal System (Nov 14, 2003)

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