# Orthopedic Designs, Inc.

- Location (FDA's records): St. Petersburg, FL
- FDA decisions: 4 (1998–2003): 4 510(k) clearances
- Product codes: HWC (2), HTN (1), JDS (1)
- Predicates its devices cite: 17 (0 its own); citations of its devices by later devices: 3 (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 whose devices it cites most
- Howmedica Corp.: 6 (https://510kreport.com/company/howmedica)
- Depuy, Inc.: 3 (https://510kreport.com/company/depuy)
- Pfizer, Inc.: 1 (https://510kreport.com/company/pfizer)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Acu Med, Inc.: 1 (https://510kreport.com/company/acu-med)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Aap Implantate AG: 1 (https://510kreport.com/company/aap-implantate)

## Firms that cite its devices most
- Orthopedic Designs, Inc. (Odi): 2 (https://510kreport.com/company/orthopedic-designs-odi)
- Orthopedic Designs North America, Inc.: 1 (https://510kreport.com/company/orthopedic-designs-north-america)

## Its most-cited devices
- K014189: Odi Talon Intramedullary Hip Nail (2002), cited by 2
- K984331: Odi Ultimate Compression Hip Screw (1999), cited by 1

## Recent decisions
- K030619: Odi 7.0MM Cannulated Screw System (Apr 1, 2003)
- K014189: Odi Talon Intramedullary Hip Nail (Mar 21, 2002)
- K984331: Odi Ultimate Compression Hip Screw (Jan 20, 1999)
- K972722: Ultimate Compression Screw System (Jan 23, 1998)

Source page: https://510kreport.com/company/orthopedic-designs