Hangzhou Jimushi Meditech Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Hangzhou Jimushi Meditech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Intermittent nelaton catheter for single use, Jimushi Sterile Urethral Catheter for single use
3
Total
3
Cleared
0
Denied
Hangzhou Jimushi Meditech Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Hangzhou, CN.
Latest FDA clearance: Jun 2026. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Hangzhou Jimushi Meditech Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Vee Care (Asia) Limited as regulatory consultant.
FDA 510(k) Regulatory Record - Hangzhou Jimushi Meditech Co., Ltd.
3 devices
Cleared
Jun 24, 2026
Hydrophilic coated intermittent nalaton catheter for single use-ready to use...
Gastroenterology & Urology
138d
Cleared
Apr 05, 2023
Intermittent nelaton catheter for single use
Gastroenterology & Urology
211d
Cleared
Jun 01, 2020
Jimushi Sterile Urethral Catheter for single use
Gastroenterology & Urology
132d