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Angelus Industria DE Productos Odontologicos
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INTERLIG is an FDA 510(k)-cleared medical device (K123823) manufactured by Angelus Industria DE Productos Odontologicos. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 30, 2013. Regulation: 8.