Syneron, Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Syneron, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Syneron, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Historical record: 2 cleared submissions from 2011 to 2012. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Syneron, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Syneron, Ltd.
2 devices