Suzhou Kangli Orthopaedics Instrument Co., Ltd. is one of 2136 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Suzhou Kangli Orthopaedics Instrument Co., Ltd. - FDA 510(k) Cleared ...
Recent clearances: KangLi pedical screw spinal system, Kangli Locking Plate System, KANGLI PEDICLE SCREW SPINAL SYSTEM
3
Total
3
Cleared
0
Denied
Suzhou Kangli Orthopaedics Instrument Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Historical record: 3 cleared submissions from 2014 to 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Suzhou Kangli Orthopaedics Instrument Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Yarui Consultant Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Suzhou Kangli Orthopaedics Instrument Co., Ltd.
3 devices