Burton
Country not established
- Devices
- 1
What Burton makes
Burton manufactures the FiberLume, a device designed for fiber-optic imaging in medical procedures, enabling real-time visualization of internal anatomical structures.
The FiberLume is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fiberlume Ref K901108
510(k) 510(k)
Frequently asked questions
How many devices does Burton have in the registry?
The registry currently lists 1 device for Burton. Devices recorded under merged duplicate company entries are counted once.
Which registries list Burton's devices?
Among its 1 most recently registered device, Burton has devices listed in FDA 510(k) (1 device).
What risk classes do Burton's devices fall under?
Among its 1 most recently registered device, the classes recorded for Burton's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Burton in the registry?
The most recently registered devices listed for Burton include FIBERLUME.