# Osteo Technology, Inc.

- Location (FDA's records): Timonium, MD
- FDA decisions: 18 (1992–1994): 18 510(k) clearances
- Product codes: JDI (7), JWH (2), HSB (1), HTY (1), LPH (1), JDG (1), KWT (1), KWA (1), JDL (1), JDQ (1), GRF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ortho Solutions Limited: 1 (https://510kreport.com/company/ortho-solutions)

## Its most-cited devices
- K925447: Oti Orthopedic Wire System (1993), cited by 1

## Recent decisions
- K926156: Replica (TM) Total Hip System (Mar 9, 1994)
- K922859: Anatomical Type Knee System (Sep 23, 1993)
- K922869: Total Condylat Type Knee System (Jul 13, 1993)
- K925447: Oti Orthopedic Wire System (Jun 29, 1993)
- K926213: Modified Zickel Intramedullary Rod System (Jun 17, 1993)
- K922861: Biometric Screw Fixation Cup (May 12, 1993)
- K922870: Three Spike Cup (Apr 8, 1993)
- K925301: Oti Orthopedic Fastener System (Mar 16, 1993)

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