Shenzhen Changkun Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Changkun Technology Co., Ltd. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jun 26, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances7Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K250070Electric breast pump (MY-375,MY-376,MY-378,MY-379,MY-380,V3)Jun 26, 2026
K252552Pelvic Floor Rehabilitation Therapy Device (PD2301/PD2302/PD2303)May 6, 2026
K231595Electric Breast PumpOct 26, 2023
K221798Finger Pulse Oximeter, Model: X1906PMay 4, 2023
K193387Arm Electronic SphygmomanometerJan 27, 2021
K193386Wrist Electronic SphygmomanometerJan 27, 2021
K193253Infrared Thermometer, Model Number CK-T1501, CK-T1502, CK-T1503Jun 17, 2020

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.