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
 

 
 
3 records meeting your search criteria returned- Product Code: KXA Patient Problem: Local Reaction Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER SWITZERLAND MANUFACTURING GMBH DUROM ACETABULAR COMPONENT 12/09/2020
ZIMMER BIOMET, INC. UNKNOWN STEM 10/11/2019
ZIMMER GMBH DUROM CUP HIP IMPLANT 05/15/2019
-
-