Hangzhou AGS MedTech Co., Ltd.

FDA Regulatory Profile

Hangzhou AGS MedTech Co., Ltd. appears in FDA public data with 0 recalls, 18 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 24, 2026.

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253393Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019 June 24, 2026
K252270HemoclipApril 8, 2026
K252271HemoclipNovember 12, 2025
K241704Endoscopic Water PumpMarch 20, 2025
K222421SphincterotomeMay 3, 2023
K221713Polypectomy SnareMarch 3, 2023
K213143HemoclipJuly 12, 2022
K213578Balloon Dilatation CatheterApril 6, 2022
K211787HemoclipMarch 3, 2022
K210406Bipolar Coagulation ForecepsOctober 5, 2021
K201121SphincterotomeFebruary 5, 2021
K202237Locking deviceDecember 23, 2020
K201509Disposable Stone Extraction basketDecember 16, 2020
K192342Electrosurgical System (Electrosurgical Generator with Bipolar polypectomy snare combination and SinMay 21, 2020
K200173Stone Retrieval BalloonMay 1, 2020
K190032Disposable Sclerotherapy NeedleFebruary 27, 2020
K172729Polypectomy SnareMay 21, 2018
K172727HemoclipApril 16, 2018