Stryker Craniomaxillofacial (Cmf)
Country not established
- Devices
- 4
What Stryker Craniomaxillofacial (Cmf) makes
Stryker Craniomaxillofacial manufactures customizable and surgeon-specific reconstruction plates for mandibular (jawbone) repairs, including tailored mandible reconstruction plates and pre-contoured fixation systems designed for craniofacial and maxillofacial surgical applications.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company’s products are listed in the FDA’s 510(k) registry, reflecting compliance with US medical device regulations.
Catalogue
Stryker Twist Drills Ref K070876
Regimes: 510(k) Registry: 510(k)Stryker Facial iD System Ref K232350
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stryker Craniomaxillofacial (Cmf) have in the registry?
The registry currently lists 4 devices for Stryker Craniomaxillofacial (Cmf). Devices recorded under merged duplicate company entries are counted once.
Which registries list Stryker Craniomaxillofacial (Cmf)'s devices?
Among its 4 most recently registered devices, Stryker Craniomaxillofacial (Cmf) has devices listed in FDA 510(k) (4 devices).
What risk classes do Stryker Craniomaxillofacial (Cmf)'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Stryker Craniomaxillofacial (Cmf)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stryker Craniomaxillofacial (Cmf) in the registry?
The most recently registered devices listed for Stryker Craniomaxillofacial (Cmf) include STRYKER TWIST DRILLS, Stryker Facial iD System, THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM and Stryker Cutomized Mandible Recon Plate; Stryker Surgeon iD Mandible Recon Plate.