Leoni Fiber Optics, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Leoni Fiber Optics, Inc. has 1 FDA 510(k) cleared medical devices. Based in Williamsburg, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Leoni Fiber Optics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group, Us, Inc. as regulatory consultant.
1 devices