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HANS BIOMED CORP receives approval from FDA

Wednesday, 15 Jan 2014 08:28pm EST 

HANS BIOMED CORP:Says received an approval from Food and Drug Administration (FDA), the United States, for SurFuse Gel/Putty, ExFuse Gel/Putty, which is a dental demineralized bone matrix (DBM) product for bone graft.Says 510(K) number of K130235. 

Company Quote

-200.0 -0.89%
27 Mar 2015