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Omni Life Science, Inc.
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APEX-LNK POLY ACETABULAR CUP LINERS is an FDA 510(k)-cleared medical device (K073150) manufactured by Omni Life Science, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 26, 2008. Regulation: 8.