
Karl Leibinger GmbH U. Co. KG
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KLS-MARTIN MANDIBULAR FRACTURE/RECONSTRUCTION SYSTEM is an FDA 510(k)-cleared medical device (K950045) manufactured by Karl Leibinger GmbH U. Co. KG. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 22, 1995. Regulation: 8.