
Biomet Microfixation
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Biomet Microfixation OmniMax MMF System is an FDA 510(k)-cleared medical device (K202969) manufactured by Biomet Microfixation. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 4, 2021. Regulation: 8.