Medical Device Manufacturer · CN , Hangzhou

Hangzhou AGS MedTech Co., Ltd. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 2018

Recent clearances: Hemoclip (511 series, 543 series), Single-use Balloon Dilatation Catheter (AG-5251-083018 AG-5251-085518 AG-5251-088018 AG-5251-083019 AG-5251-085519 AG-5251-088019 AG-5251-083021 AG-5251-085521 AG-5251-088021 AG-5251-083024 AG-5251-085524 AG-5251-088024 AG-5251-103018 AG-5251-105518 AG-5251-108018 AG-5251-103019 AG-5251-105519 AG-5251-108019 AG-5251-103021 AG-5251-105521 AG-5251-108021 AG-5251-103024 AG-5251-105524 AG-5251-108024 AG-5251-123018 AG-5251-125518 AG-5251-128018 AG-5251-123019 AG-5251-125519 AG-5251-128019, Hemoclip

Total

Cleared

Denied

Hangzhou AGS MedTech Co., Ltd. has 19 FDA 510(k) cleared gastroenterology & urology devices. Based in Hangzhou, CN.

Latest FDA clearance: Aug 2026. Active since 2018.

Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Shanghai Thinkwell Consulting Co., Ltd. as regulatory consultant.

Hangzhou AGS MedTech Co., Ltd. is one of 2114 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.