Suzhou Kangli Orthopaedics Instrument Co., Ltd.

FDA Regulatory Profile

Suzhou Kangli Orthopaedics Instrument Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 24, 2014.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142290KangLi pedical screw spinal systemNovember 24, 2014
K133840Kangli Locking Plate SystemJuly 29, 2014
K140053KANGLI PEDICLE SCREW SPINAL SYSTEMJune 26, 2014