Not currently registered with FDA under this name
Stryker Craniomaxillofacial
Portage, MI, United States. Named as applicant on 2 dental 510(k) clearances between 2010 and 2024. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22010–2024
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Stryker Craniomaxillofacial as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 13 Jan 2024 | K232350 | Stryker Facial iD System | JEY Bone Plate |
| 15 Jan 2010 | K092743 | THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM | JEY Bone Plate |
Some of these clearances are listed with FDA today by another company: Stryker (1).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.