Home / Companies / Zhejiang Kindly Medical Device Co., Ltd.

Zhejiang Kindly Medical Device Co., Ltd.

FDA Regulatory Profile

Zhejiang Kindly Medical Device Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 2, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K252899Female Culture Device; Male Culture Device; Transfer Device; Access DeviceJun 2, 2026
K233037Sterile Hypodermic Needles for Single UseDec 12, 2023

FDA data resources