# Osteo-Technology Intl., Inc.

- Location (FDA's records): Timonium, MD
- FDA decisions: 3 (1993–1995): 3 510(k) clearances
- Product codes: HRS (1), JDI (1), LPH (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
- K951741: Replica Total Hip System (Aug 7, 1995)
- K935012: Biometric Total Hip System (Mar 7, 1994)
- K925571: Oti European Compression System (Jul 13, 1993)

Source page: https://510kreport.com/company/osteo-technology-intl