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 
 
 
28 records meeting your search criteria returned- Product Code: DZE Product Problem: Device-Device Incompatibility Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY2 4.2DX10L 3.5MMD PLATFORM 02/21/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC INTERACTIVE 5.0MMDX8MML SBM 3.4MMD PLATF 02/20/2018
IMPLANT DIRECT SYBRON MANUFACTURING LLC INTERACTIVE 3.7MMDX10MML SBM 3.0MMD PLAT 02/20/2018
IMPLANT DIRECT LLC LEGACY¿4 IMPLANT 01/26/2018
IMPLANT DIRECT LLC INTERACTIVE® IMPLANT 12/27/2017
IMPLANT DIRECT LLC LEGACY¿3 IMPLANT 11/20/2017
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY4 IMPLANT 09/05/2017
BIOMET 3I OSSEOTITE® TAPERED CERTAIN® IMPLANT 4 X 11/24/2015
-
-