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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
107 records meeting your search criteria returned- Product Code: KXA Patient Problem: Hypersensitivity/Allergic reaction Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNKNOWN RECAP HIP SYSTEM 06/30/2022
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/26/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/13/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/11/2020
DEPUY ORTHOPAEDICS INC US UNK HIP FEMORAL STEM SUMMIT 03/09/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL HEAD 03/05/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/05/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/04/2020
DEPUY INTERNATIONAL LTD - 8010379 TAPER SLEEVE ADAPTER 12/14 +2 03/04/2020
DEPUY INTERNATIONAL LTD - 8010379 ASR ACETABULAR IMPLANT 62 03/04/2020
-
-