
Bicon, Inc.
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THE 6.0 X 8.0MM DENTAL IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K972417) manufactured by Bicon, 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 September 16, 1997. Regulation: 8.