
Implant Integration Systems, Inc.
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DUAL INTEGRATOR DENTAL IMPLANT ACCESSORIES is an FDA 510(k)-cleared medical device (K962610) manufactured by Implant Integration Systems, 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 October 17, 1996. Regulation: 8.