# Stryker Craniomaxillofacial

- Location (FDA's records): Portage, MI
- FDA decisions: 3 (2007–2024): 3 510(k) clearances
- Product codes: JEY (2), HBE (1)
- Predicates its devices cite: 8 (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 Leibinger, Inc.: 2 (https://510kreport.com/company/howmedica-leibinger)
- KLS-Martin L.P.: 2 (https://510kreport.com/company/kls-martin)
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Walter Lorenz Surgical, Inc.: 1 (https://510kreport.com/company/walter-lorenz-surgical)

## Firms that cite its devices most
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)

## Its most-cited devices
- K092743: The Leibinger Advance Internal Midface Distraction System (2010), cited by 2

## Recent decisions
- K232350: Stryker Facial iD System (Jan 13, 2024)
- K092743: The Leibinger Advance Internal Midface Distraction System (Jan 15, 2010)
- K070876: Stryker Twist Drills (Apr 27, 2007)

Source page: https://510kreport.com/company/stryker-craniomaxillofacial