Yilink (Tianjin) Biotechnology Co., Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Yilink (Tianjin) Biotechnology Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Tianjin, CN.
Latest FDA clearance: Oct 2024. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Yilink (Tianjin) Biotechnology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Chenhe Medical Consulting Co., Ltd. as regulatory consultant.
3 devices