Ushare Medical, Inc. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Ushare Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Polysaccharide Hemostatic Powder (HP-2, HP-3, HP-5), Biopsy Needle
2
Total
2
Cleared
0
Denied
Ushare Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Zhuhai, CN.
Latest FDA clearance: May 2024. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ushare Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Shanghai SUNGO Management Consulting Co., Ltd. and Shenzhen Joyantech Consulting Co., Ltd..
FDA 510(k) Regulatory Record - Ushare Medical, Inc.
2 devices