Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 
 
41 records meeting your search criteria returned- Product Code: DZA Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAILLEFER INSTRUMENTS HOLDING SA GATES GLIDDEN DRILL 06/18/2015
DENTSPLY MAILLEFER GP PLUGGER 06/10/2015
INTEGRA YORK, PA INC. 301 ELEV. 06/19/2014
INTEGRA YORK, PA INC 301 ELEV 06/19/2014
INTEGRA YORK, PA INC. 301 ELEV. 06/19/2014
INTEGRA YORK, PA INC. 301 ELEV. 06/16/2014
INTEGRA YORK, PA INC. 301 ELEV. 06/16/2014
DENTSPLY MAILLEFER GATES GLIDDEN DRILL 05/15/2014
DENTSPLY MAILLEFER GATES GLIDDEN DRILL 05/15/2014
INTEGRA YORK PA INC 301 ELEV. 05/12/2014
-
-