
Surgikor, LLC
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Surgikor Fixation One, Abutment Blanks and Abutments is an FDA 510(k)-cleared medical device (K240803) manufactured by Surgikor, LLC. 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 11, 2024. Regulation: 8.