Hunan Vathin Medical Instrument Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
17
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250232Vathin® Video Bronchoscope SystemJuly 25, 2025
K251599Single-use Ureteral Access SheathJuly 3, 2025
K250785Single-use Flexible UreteroscopeMay 6, 2025
K243117Digital Video ProcessorJanuary 29, 2025
K242416Single-use Flexible Bronchoscope: BC-E1C10, BC-E1C11, BC-E1C12, BC-E1E10, BC-E1E11, BC-E1E12, BC-E1HJanuary 16, 2025
K242535Single-use Flexible Cystoscope (CY-E2E01, CY-E2E01R, CY-E2F01, CY-E2F01R, CY-E2G01, CY-E2G01R, CY-S2December 18, 2024
K241612Video Bronchoscope System; Single-use Flexible Bronchoscope (BC-S1E00-L, BC-S1H00-L, BC-S1J00-L, BC-October 29, 2024
K240167Single-use Ureteral Access SheathOctober 8, 2024
K241434Video Ureteroscope SystemOctober 4, 2024
K231135Video Ureteroscope SystemJanuary 17, 2024
K230536Single-use Flexible Rhinolaryngoscope; Digital Video MonitorJune 14, 2023
K230200Single-Use Flexible UreteroscopeMay 18, 2023
K223836Vathin® Video Bronchoscope SystemMay 15, 2023
K221580Single-Use Flexible CystoscopeNovember 18, 2022
K221581Single-Use Flexible RhinolaryngoscopeNovember 18, 2022
K213635Vathin Video Bronchoscope SystemFebruary 28, 2022
K191828Vathin Video Bronchoscope SystemFebruary 13, 2020