# Orthodyne, Inc.

- Location (FDA's records): Orlando, FL
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: HSB (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Howmedica Corp.: 1 (https://510kreport.com/company/howmedica)
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)

## Firms that cite its devices most
- Orthofix, Inc.: 1 (https://510kreport.com/company/orthofix)
- Inter-Os Technologies: 1 (https://510kreport.com/company/inter-os-technologies)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Ellipse Technologies, Inc.: 1 (https://510kreport.com/company/ellipse-technologies)

## Its most-cited devices
- K010322: Iskd (Intramedullary Skeletal Kinetic Distractor) (2001), cited by 4

## Recent decisions
- K010322: Iskd (Intramedullary Skeletal Kinetic Distractor) (May 2, 2001)

Source page: https://510kreport.com/company/orthodyne