• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
 1 
 2 
 > 
 
12 records meeting your search criteria returned- Product Code: EMA Patient Problem: Reaction Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DENTSPLY CAULK INTEGRITY TEMPGRIP 01/06/2020
3M VITREBOND 02/22/2017
DENTSPLY DETREY GMBH KALSOGEN PLUS 11/11/2016
IVOCLAR VIVADENT AG TELIO CS LINK 10/05/2016
DENTSPLY CAULK INTEGRITY TEMPGRIP 11/19/2015
DENTSPLY CAULK INTEGRITY TEMPGRIP 07/23/2015
DENTSPLY CAULK IRM ZOE INTERMEDIATE RESTORATIVE MATERIA 06/18/2015
DENTSPLY CAULK IRM ZOE INTERMEDIATE RESTORATIVE MATERIA 06/18/2015
DENTSPLY CAULK IRM ZOE INTERMEDIATE RESTORATIVE MATERIA 02/11/2015
3M RELYX PLUS LUSTING CEMENT ESPE 12/20/2014
-
-