
Lucero Medical, LLC
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ENDURAMESH, MODEL 762.XXX is an FDA 510(k)-cleared medical device (K093207) manufactured by Lucero Medical, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 25, 2010. Regulation: 8.