Sichuan Qianli-Beoka Medical Technology, Inc. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Sichuan Qianli-Beoka Medical Technology, Inc. - FDA 510(k) Cleared De...
Recent clearances: Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6)
1
Total
1
Cleared
0
Denied
Sichuan Qianli-Beoka Medical Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chengdu, CN.
Latest FDA clearance: Feb 2025. Active since 2025. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Sichuan Qianli-Beoka Medical Technology, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Reanny Medical Devices Mgmt Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Sichuan Qianli-Beoka Medical Technology, Inc.
1 devices