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Biopro, Inc.
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BIOPRO BIPOLAR HEAD, MODELS 18130-18152 is an FDA 510(k)-cleared medical device (K082705) manufactured by Biopro, 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 December 14, 2008. Regulation: 8.