# Orthopedic Designs North America, Inc.

- Location (FDA's records): Tampa, FL
- FDA decisions: 4 (2011–2022): 4 510(k) clearances
- Product codes: HSB (3), HWC (1)
- Predicates its devices cite: 12 (0 its own); citations of its devices by later devices: 2 (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 Osteonics Corp.: 6 (https://510kreport.com/company/howmedica-osteonics)
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Orthopedic Designs, Inc.: 1 (https://510kreport.com/company/orthopedic-designs)
- Orthopedic Designs, Inc. (Odi): 1 (https://510kreport.com/company/orthopedic-designs-odi)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)

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

## Its most-cited devices
- K173255: Talon DistalFix Humeral Nail (2018), cited by 1
- K111352: Talon Distalfix Proximal Femoral Nail (2011), cited by 1

## Recent decisions
- K210146: Cannulated Compression Device System (Apr 13, 2022)
- K173255: Talon DistalFix Humeral Nail (Feb 22, 2018)
- K152295: Talon DistalFix Antegrade/Retrograde Femoral Nail (Nov 3, 2015)
- K111352: Talon Distalfix Proximal Femoral Nail (Aug 22, 2011)

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