Syneron Beauty is one of 19031 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Syneron Beauty - FDA 510(k) Cleared Devices
Recent clearances: TANDA MINI SKINCARE SYSTEM, TANDA PEARL, ULTRAWYTE, PEARL
2
Total
2
Cleared
0
Denied
Syneron Beauty has 2 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Syneron Beauty Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syneron Beauty
2 devices