KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERS

KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERS is an FDA 510(k)-cleared medical device (K961381) manufactured by The Emerging Technologies Group. 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 8, 1997. Regulation: 8.