
Sie Ag,Surgical Instument Engineering
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FEMTO LDV is an FDA 510(k)-cleared medical device (K112154) manufactured by Sie Ag,Surgical Instument Engineering. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 15, 2012. Regulation: 8.