Wavelight Laser Technologie AG - FDA 510(k) Cleared Devices

Wavelight Laser Technologie AG has 8 FDA 510(k) cleared medical devices. Based in North Reading, US.

Historical record: 8 cleared submissions from 2004 to 2006. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Wavelight Laser Technologie AG Filter by specialty or product code using the sidebar.

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