K&J Consulting Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
K&J Consulting Corporation - FDA 510(k) Cleared Devices
Recent clearances: FaSet Fixation System, UNITY Sacroiliac Joint Fixation System, Huvex Interspinous Fixation System, and AEON-C™ Stand Alone System, K&J IVA (ACIF, DLIF, PLIF, TLIF, ALIF) PEEK Cage
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.
Regulatory submissions have been managed by RQMIS, Inc. and Eerkie Corporation.
FDA 510(k) Regulatory Record - K&J Consulting Corporation
2 devices