Zhejiang Soudon Medical Technology Co., Ltd.

FDA Regulatory Profile

Zhejiang Soudon Medical Technology Co., Ltd. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 8, 2026.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253013Disposable Stone Retrieval Balloon CatheterMay 8, 2026
K253056Disposable Stone Extraction BasketApril 3, 2026
K232450Disposable Hemostatic ClipsJanuary 26, 2024
K232442Disposable Endoscope Injection NeedlesNovember 9, 2023
K232476Disposable SphincterotomeNovember 7, 2023