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Bredent GmbH & Co. KG
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K240735
visio.lign color, visio.lign shield
December 12, 2024
K152113
BioHPP - breCAM.BioHPP
July 21, 2016
K101064
BREDENT NOVO.LIGN A/ BREDENT NOVO.LIGN P
September 14, 2010