Medical Device Manufacturer · US , Wesford , MA

Cynosure, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2020

Total

Cleared

Denied

Cynosure, LLC has 8 FDA 510(k) cleared medical devices. Based in Wesford, US.

Latest FDA clearance: Jun 2026. Active since 2020. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Cynosure, LLC Filter by specialty or product code using the sidebar.

Cynosure, LLC is one of 16094 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cynosure, LLC

8 devices

1-8 of 8