
W and R Investments Dba Laser Engineering
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ULTRALASE FLEXIBLE CO2 LASER WAVEGUIDE is an FDA 510(k)-cleared medical device (K112166) manufactured by W and R Investments Dba Laser Engineering. 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 October 20, 2011. Regulation: 8.