Cynosure is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cynosure - FDA 510(k) Cleared Devices
Recent clearances: SculpSure
1
Total
1
Cleared
0
Denied
Cynosure has 1 FDA 510(k) cleared medical devices. Based in Wesford, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cynosure Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cynosure
1 devices