Acotec Scientific Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Acotec Scientific Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Cedar™ Endovenous Radiofrequency Catheter (ERA-C70-US)
1
Total
1
Cleared
0
Denied
Acotec Scientific Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Beijing, CN.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Acotec Scientific Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Fabrica Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Acotec Scientific Co., Ltd.
1 devices