3M Espe Dental Products

FDA Regulatory Profile

3M Espe Dental Products appears in FDA public data with 0 recalls, 12 510(k) clearances, 8 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 10, 2023.

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
8
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K2313383M™ Clinpro™ Clear 2.1% Sodium Fluoride TreatmentMay 10, 2023
K2302703M™ VitCal Liner/BaseFebruary 6, 2023
K1911223M RelyX Pediatric Resin Modified Glass Ionomer CementMay 29, 2019
K1834763M Filtek Universal RestorativeJanuary 2, 2019
K141081FILTEK BULK FILL POSTERIOR RESTROATIVEMay 8, 2014
K120453FILTEK BULK FILL FLOWABLE RESTORATIVEMarch 19, 2012
K111185RELYX LUTING PLUS AUTOMIXMay 5, 2011
K110131LAVA ULTIMATE CAD/CAM RESTORATIVE FOR CEREC / E4D, LAVA ULTIMATE IMPLANT CROWN RESTORATIVEJanuary 21, 2011
K092141VANISH VARNISH, 5% SODIUM FLUORIDE WHITE VARNISHMarch 10, 2010
K073395GILB-2, GLASS IONOMER PROTECTIVE COATINGJanuary 17, 2008
K070956SEA2 SELF ETCH ADHESIVEMay 22, 2007
K062292UNICEMOctober 25, 2006