Cyberorthology, Inc.
Country not established
- Devices
- 1
What Cyberorthology, Inc. makes
Cyberorthology, Inc. manufactures the Carbon Fiber Composite Circular Fixation (CirFix) Device, a half-ring orthopedic fixation system designed for bone stabilization.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Cyberorthology, Inc. have in the registry?
The registry currently lists 1 device for Cyberorthology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cyberorthology, Inc.'s devices?
Among its 1 most recently registered device, Cyberorthology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cyberorthology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cyberorthology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cyberorthology, Inc. in the registry?
The most recently registered devices listed for Cyberorthology, Inc. include CARBON FIBER COMPOSITE CIRCULAR FIXATION (CIRFIX) DEVICE (HALF RING).