• 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
 

 
 
8 records meeting your search criteria returned- Product Code: ETA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC XOMED INC. PROSTHESIS - STAPES 05/30/2023
MEDTRONIC XOMED INC. PROSTHESIS - UNIVERSAL TITANIUM PROSTHES 04/19/2023
MEDTRONIC XOMED INC. PROSTHESIS 12/04/2017
MEDTRONIC XOMED INC. PROSTHESIS 08/04/2017
MEDTRONIC XOMED INC. PROSTHESIS 08/04/2017
MEDTRONIC XOMED INC. PROSTHESIS - POLYCEL 11/28/2016
MEDTRONIC XOMED INC. PROSTHESIS - POLYCEL 11/28/2016
MEDTRONIC XOMED INC. PROSTHESIS - POLYCEL 11/28/2016
-
-