
The Implant Center of the Palm Beaches
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KIS II LG HEX SCREW & CYLINDER IMPLANTS is an FDA 510(k)-cleared medical device (K953558) manufactured by The Implant Center of the Palm Beaches. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 18, 1995. Regulation: 8.