
Intra-Lock International, Inc.
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INTRA-LOCK DENTAL IMPLANTS WITH BLOSSOM is an FDA 510(k)-cleared medical device (K103194) manufactured by Intra-Lock International, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 20, 2011. Regulation: 8.