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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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