FDA 510(k) Applications Submitted by Bredent GmbH & Co.KG

FDA 510(k) Number Submission Date Device Name Applicant
K101064 04/16/2010 BREDENT NOVO.LIGN A/ BREDENT NOVO.LIGN P BREDENT GMBH & CO.KG
K152113 07/29/2015 BioHPP - breCAM.BioHPP Bredent GmbH & Co.KG


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