Hangzhou Qiantang Longyue Biotechnology Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Hangzhou Qiantang Longyue Biotechnology Co., Ltd. - FDA 510(k) Cleare...
Recent clearances: Vial Adapter, Vent Vial Adapter, Filter Needle for Single Use
5
Total
5
Cleared
0
Denied
Hangzhou Qiantang Longyue Biotechnology Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Hangzhou, CN.
Latest FDA clearance: Jun 2026. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Lingfu Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Hangzhou Qiantang Longyue Biotechnology Co., Ltd.
5 devices
Cleared
Jun 05, 2026
Vial Adapter
General Hospital
126d
Cleared
Jul 26, 2024
Vent Vial Adapter
General Hospital
301d
Cleared
May 10, 2024
Filter Needle for Single Use
General Hospital
224d
Cleared
May 01, 2024
Vial Adapter with Filter
General Hospital
215d
Cleared
Mar 10, 2023
Vial Adapter
General Hospital
183d