# Orthonetx, Inc.

- Location (FDA's records): Superior, CO
- FDA decisions: 1 (2005–2005): 1 510(k) clearance
- Product codes: KTT (1)
- Predicates its devices cite: 5 (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

## Firms whose devices it cites most
- Inter-Os Technologies: 2 (https://510kreport.com/company/inter-os-technologies)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Walter Lorenz Surgical, Inc.: 1 (https://510kreport.com/company/walter-lorenz-surgical)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Recent decisions
- K051162: Generos SB Small Bone Distraction Implant (Jul 19, 2005)

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