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Ortho Kinematics, Inc.
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THE KINEGRAPH VMA SOFTWARE, THE MOTION NORMALIZER PATIENT HANDLING AND DATA COLLECTION DEVICE is an FDA 510(k)-cleared medical device (K112109) manufactured by Ortho Kinematics, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 21, 2011. Regulation: 8.