Fxdevices
Country not established
- Devices
- 4
What Fxdevices makes
Fxdevices makes the POGO Screw, a bone fixation device, and its associated instrumentation tray, as well as the Lagwire System, which is used for spinal stabilization.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Pogo Screw Ref K092189
510(k) 510(k)Pogo Screw Instrumentation Tray Ref K091806
510(k) 510(k)Lagwire System Ref K070393
510(k) 510(k)Pogo Screw Ref K080649
510(k) 510(k)
Frequently asked questions
How many devices does Fxdevices have in the registry?
The registry currently lists 4 devices for Fxdevices. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fxdevices's devices?
Among its 4 most recently registered devices, Fxdevices has devices listed in FDA 510(k) (4 devices).
What risk classes do Fxdevices's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Fxdevices's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fxdevices in the registry?
The most recently registered devices listed for Fxdevices include POGO SCREW, POGO SCREW INSTRUMENTATION TRAY and LAGWIRE SYSTEM.