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Lasering S.R.L.
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VELURE FAMILY OF DIODE LASERS AND DELIVERY DEVICE ACCESSORIES is an FDA 510(k)-cleared medical device (K063396) manufactured by Lasering S.R.L.. 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 16, 2007. Regulation: 8.