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 
 6 
 7 
 8 
 9 
 10 
 > 
 
103 records meeting your search criteria returned- Product Code: DZE Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 4 IMPLANT 10/09/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 4 IMPLANT 10/09/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 4 IMPLANT 10/09/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 2 IMPLANT 09/28/2018
NEODENT - JJGC S.A. CM DRIVE ACQUA IMPLANT 5.0X8 09/13/2018
NEODENT - JJGC S.A. WS TITAMAX IMPLANT 4.0X6 09/10/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 2 IMPLANT 08/15/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY 3 IMPLANT 08/09/2018
DENTSPLY IMPLANTS MANUFACTURING GMBH ANKYLOS C/X 07/31/2018
DENTSPLY IMPLANTS MANUFACTURING GMBH ANKYLOS C/X 04/30/2018
-
-