Shanghai SeeGen Photoelectric Technology Co., Ltd.

FDA Regulatory Profile

Shanghai SeeGen Photoelectric Technology Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 30, 2026.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252457Disposable Distal End Tape HoodJanuary 30, 2026
K243535Flexible Video-Choledochoscope (CHV-110J-U); Flexible Video-Choledochoscope (CHV-US120J-U)March 7, 2025
K241532Flexible Video-Choledo-Cysto-Ureteroscope System (PL-2100)October 22, 2024
K222499Disposable Endoscope Valves KitNovember 22, 2023
K222261Flexible Video-Choledochoscope SystemApril 20, 2023
K211686Flexible Video-Choledo-Cysto-Ureteroscope SystemFebruary 22, 2022