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Duerr Dental AG
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K172007
CamX Triton HD Proxi Head
November 22, 2017
K170733
ScanX Intraoral View
May 1, 2017
K161444
DBSWIN and VistaEasy Imaging Software
June 21, 2016