Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Lutronic Corporation
Free shipping on orders over $99 · 30-day returns
LUTRONIC CORPORATION ECO2 PLUS, DENTA III AND III+ AND SP III LASER SYSTEMS is an FDA 510(k)-cleared medical device (K100610) manufactured by Lutronic Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 19, 2011. Regulation: 8.