SHENZHEN SUPERLINE TECHNOLOGY CO., LTD. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
SHENZHEN SUPERLINE TECHNOLOGY CO., LTD. - FDA 510(k) Cleared Devices
Recent clearances: Alpha Endo Handpiece (Alpha Endo), Electronic Apex Locator (Alpha Apex I)
2
Total
2
Cleared
0
Denied
SHENZHEN SUPERLINE TECHNOLOGY CO., LTD. has 2 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by SHENZHEN SUPERLINE TECHNOLOGY CO., LTD. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pureid Medical Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.
2 devices