# Dgimed Ortho, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 3 (2009–2014): 3 510(k) clearances
- Product codes: HSB (3)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 1 (1 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
- Richards Medical Co., Inc.: 1 (https://510kreport.com/company/richards-medical)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)

## Its most-cited devices
- K091309: Revolution Femoral Intramedullary Nail System, Model Dgooxx (2009), cited by 1

## Recent decisions
- K132830: Distalock Tibial IM Nail System (Jan 6, 2014)
- K100312: Distalock Femoral Intramedullary Nail System (Apr 20, 2010)
- K091309: Revolution Femoral Intramedullary Nail System, Model Dgooxx (Nov 5, 2009)

Source page: https://510kreport.com/company/dgimed-ortho