Medical Device Manufacturer · US , Lansdale , PA

K&J Consulting Corp. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2023
3
Total
3
Cleared
0
Denied

K&J Consulting Corp. has 3 FDA 510(k) cleared medical devices. Based in Lansdale, US.

Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by K&J Consulting Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by K&J Consulting Corp.

3 devices
1-3 of 3
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All3 Orthopedic 3