
Stryker
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Stryker Upper-Face AXS screws and Mid-Face AXS screws is an FDA 510(k)-cleared medical device (K172572) manufactured by Stryker. 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 30, 2017. Regulation: 8.