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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 > 
 
20 records meeting your search criteria returned- Product Code: DZI Patient Problem: Failure of Implant Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IMPLANT DIRECT SYBRON MANUFACTURING LLC DIRECTGUIDE DRILL EXTENDER 10/18/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC DIRECTGUIDE DRILL EXTENDER 10/18/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC DLC CORTICAL BONE DRILL 3.7MMD IMPLANT 08/04/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC STEP DRILL (6-16MML) 04/19/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC STEP DRILL (6-16MML) 03/24/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC DIRECTGUIDE DRILL EXTENDER 07/18/2022
IMPLANT DIRECT SYBRON MANUFACTURING LLC DIRECTGUIDE DRILL EXTENDER 07/18/2022
IMPLANT DIRECT SYBRON MANUFACTURING LLC STEP DRILL (6-16MML) 10/12/2021
IMPLANT DIRECT SYBRON MANUFACTURING LLC STEP DRILL EXTRA LONG (6-28MML) 10/06/2021
IMPLANT DIRECT SYBRON MANUFACTURING LLC DLC STEP DRILL 4.8/4.4MM (6-16MML) 09/21/2021
-
-