K&J Consulting Corporation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
K&J Consulting Corporation has 2 FDA 510(k) cleared medical devices. Based in Lansdale, US.
Last cleared in 2023. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by K&J Consulting Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by K&J Consulting Corporation
2 devices