# Global Orthopaedic Technology, USA, Inc.

- Location (FDA's records): Oviedo, FL
- FDA decisions: 3 (2004–2005): 3 510(k) clearances
- Product codes: HRY (2), KRR (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K050473: RBK Patella Femoral Knee (Nov 14, 2005)
- K051721: Global Resurfacing Unicompartmental Knee System (Oct 26, 2005)
- K033351: Global Resurfacing Unicompartmental (Gru) Knee (Mar 11, 2004)

Source page: https://510kreport.com/company/global-orthopaedic-technology-usa