J. Leon Bilby
Country not established
- Devices
- 1
What J. Leon Bilby makes
J. Leon Bilby manufactures the M.P.I. LENS GLIDE, a device designed for intraocular lens insertion during cataract surgery, facilitating precise placement within the eye.
The company’s portfolio is regulated under Class I medical devices in the United States, with the M.P.I. LENS GLIDE listed via the FDA’s 510(k) pathway. The manufacturer operates from the US.
Catalogue
M.P.I. Lens Glide Ref K792066
510(k) 510(k)
Frequently asked questions
How many devices does J. Leon Bilby have in the registry?
The registry currently lists 1 device for J. Leon Bilby. Devices recorded under merged duplicate company entries are counted once.
Which registries list J. Leon Bilby's devices?
Among its 1 most recently registered device, J. Leon Bilby has devices listed in FDA 510(k) (1 device).
What risk classes do J. Leon Bilby's devices fall under?
Among its 1 most recently registered device, the classes recorded for J. Leon Bilby's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from J. Leon Bilby in the registry?
The most recently registered devices listed for J. Leon Bilby include M.P.I. LENS GLIDE.