Lutronic Global
LaseMD LEO Laser System
SKU K192331UPC GEX
In Stock
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IIFDA 510(k) Cleared (K192331)
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Free shipping on orders over $99 · 30-day returns
Lutronic Global
Free shipping on orders over $99 · 30-day returns
LaseMD LEO Laser System is an FDA 510(k)-cleared medical device (K192331) manufactured by Lutronic Global. 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 November 11, 2019. Regulation: 8.
