Changzhou Endoclean Medical Device Co., Ltd.

FDA Regulatory Profile

Changzhou Endoclean Medical Device Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 29, 2023.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K232244Disposable Endoscope Valves SystemNovember 29, 2023
K221310Endoscopic Clean Connecting Tubes, Endoscopic CO2 Source TubingOctober 7, 2022
K221331Disposable Endoscope Valves SystemSeptember 8, 2022