# Genesis Fracture Care, Inc.

- Location (FDA's records): Clackamas, OR
- FDA decisions: 5 (2014–2017): 5 510(k) clearances
- Product codes: HRS (5)
- Predicates its devices cite: 23 (5 its own); citations of its devices by later devices: 5 (5 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
- Zimmer, Inc.: 7 (https://510kreport.com/company/zimmer)
- Smith & Nephew, Inc.: 4 (https://510kreport.com/company/smith-nephew)
- Synthes (Usa): 3 (https://510kreport.com/company/synthes-usa)
- Hand Innovations, Inc.: 1 (https://510kreport.com/company/hand-innovations)
- DePuy Orthopaedics, Inc.: 1 (https://510kreport.com/company/depuy-orthopaedics)
- Small Bone Innovations, Inc.: 1 (https://510kreport.com/company/small-bone-innovations)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)

## Its most-cited devices
- K142938: G3 Active Plate Large Fragment System (2014), cited by 3
- K152242: G3¿ Active Plate® Large Fragment System (2015), cited by 1
- K150649: G3 Active Plate Large Fragment System (2015), cited by 1

## Recent decisions
- K171293: G3™ Active Plate® Miniature System (Oct 23, 2017)
- K160633: G3(TM) Active Plate (R) Small Fragment System (Apr 22, 2016)
- K152242: G3¿ Active Plate® Large Fragment System (Nov 24, 2015)
- K150649: G3 Active Plate Large Fragment System (Apr 30, 2015)
- K142938: G3 Active Plate Large Fragment System (Nov 26, 2014)

Source page: https://510kreport.com/company/genesis-fracture-care