K&J Consulting Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
K&J Consulting Corp. - FDA 510(k) Cleared Devices
Recent clearances: Statera-C™ Spinal System, Rexious Spinal Fixation System, Statera™ Spinal System, Statera-M™ Spinal System, FORTIS and HANA Anterior Cervical Plate System, Rex Anterior Cervical Plate System, BALTEUM™ & BALTEUM-ONE™ Lumbar Plate System, and Osprey™ Anterior Cervical Plate System
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.
510(k) submissions have been managed by Eerkie Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - K&J Consulting Corp.
3 devices