Keos - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Keos has 4 FDA 510(k) cleared medical devices. Based in Lancaster, US.
Last cleared in 2022. Active since 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Keos Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Keos
4 devices