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 
 3 
 > 
 
25 records meeting your search criteria returned- Product Code: OTD Product Problem: Activation, Positioning or Separation Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 02/09/2024
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 09/13/2023
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 11/07/2022
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 06/27/2022
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 06/14/2022
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 05/16/2022
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 04/12/2022
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 11/01/2021
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 03/26/2021
MEDTRONIC IRELAND ENDO ANCHOR SYSTEM - HELI-FX AAA 09/16/2020
-
-