Xceramusa
Country not established
- Devices
- 1
What Xceramusa makes
Xceramusa manufactures the XCERAM, a ceramic-based medical device designed for orthopedic applications, including joint replacement components and bone grafting materials. The product is engineered to provide structural support and biocompatibility in surgical procedures.
The XCERAM device falls under Class II classification and is listed in the FDA’s 510(k) registry as a regulated medical product. The company operates from the United States, adhering to domestic regulatory requirements for its distribution and use.
Catalogue
Xceram Ref K100250
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xceramusa have in the registry?
The registry currently lists 1 device for Xceramusa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xceramusa's devices?
Among its 1 most recently registered device, Xceramusa has devices listed in FDA 510(k) (1 device).
What risk classes do Xceramusa's devices fall under?
Among its 1 most recently registered device, the classes recorded for Xceramusa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xceramusa in the registry?
The most recently registered devices listed for Xceramusa include XCERAM.