Lutronic Corporation - FDA 510(k) Cleared Devices

Lutronic Corporation has 29 FDA 510(k) cleared general & plastic surgery devices. Based in North Reading, US.

Latest FDA clearance: Aug 2025. Active since 2007.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Cynosure, Inc. as regulatory consultant.