Bio2 Technologies' CLM Bioactive Scaffold receives FDA approval

Written by Anuja Vaidya | December 22, 2014 | Print  |

Bio2 Technologies received 510(k) clearance from the U.S. Food and Drug Administration for its CLM Bioactive Scaffold.

CLM is constructed from bioactive glass, a resorbable implantable material. Bio2 has successfully applied the proprietary CLM process technology to produce a rigid, osteoconductive material with an interconnected porous structure facilitating the ingrowth and remodeling of healthy bone.


Bio2 is focused on developing a number of CLM-constructed products designed for reconstructive surgery of the extremities.

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