Lifecore Biomedical's hydroxylapatite bone graft plaster, Hapset, has been cleared for use in defect restorations in maxillary, mandibular and zygomatic sites. Hapset is currently cleared by the US FDA for use only in the restoration of periodontal and extraction socket bone defects in dental surgery. The company based in Chaska, Minnesota, estimates that approximately 430,000 maxillofacial bone repair procedures are performed annually in the US.
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