Beijing Keyi Medical Device Technology Co., Ltd.

FDA Regulatory Profile

Beijing Keyi Medical Device Technology Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 19, 2024.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K230120KeYi Total Knee SystemApril 19, 2024
K191826KeYi Total Hip SystemMay 14, 2020
K190567KeYi Spinal Fixation SystemMay 8, 2019
K162380Locking Plate SystemMay 2, 2017