• 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 
 3 
 4 
 5 
 6 
 7 
 > 
 
63 records meeting your search criteria returned- Product Code: KLE Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HERAEUS KULZER GMBH GLUMA DESENSITIZER 02/03/2016
HERAEUS KULZER GMBH GLUMA DESENSITIZER 01/13/2016
HERAEUS KULZER GMBH GLUMA DESENSITIZER 01/13/2016
DENTSPLY CAULK PRIME & BOND ELECT UNIVERSAL DENTAL ADHE 12/23/2015
KERR CORPORATION OPTIBOND XTR 12/17/2015
DENTSPLY CAULK PRIME & BOND ELECT UNIVERSAL DENTAL ADHE 12/11/2015
HERAEUS KULZER GMBH IBOND TOTAL ETCH 10/30/2015
HERAEUS KULZER GMBH GLUMA DESENSITIZER 10/30/2015
HERAEUS KULZER GMBH GLUMA DESENSITIZER 10/14/2015
HERAEUS KULZER GMBH GLUMA DESENSITIZER 09/24/2015
-
-