• 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 
 > 
 
24 records meeting your search criteria returned- Product Code: KWA Patient Problem: Itching Sensation Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN HEAD 12/03/2021
ZIMMER BIOMET, INC. UNKNOWN SHELL 12/03/2021
DEPUY ORTHOPAEDICS INC US PINNACLE MTL INS NEUT36IDX52OD 03/12/2021
ZIMMER BIOMET ZIMMER DUROM METAL-ON-METAL HIP DEVICE 02/12/2020
ZIMMER BIOMET ZIMMER DUROM METAL-ON-METAL HIP DEVICE 02/12/2020
DEPUY INTERNATIONAL LTD - 8010379 TOTAL ASR FEM IMP SIZE 45 07/29/2019
DEPUY INTERNATIONAL LTD - 8010379 ASR ACETABULAR IMPLANT 50 07/29/2019
DEPUY ORTHOPAEDICS, INC. 1818910 PINNACLE MTL INS NEUT36IDX52OD 06/28/2019
DEPUY ORTHOPAEDICS, INC. 1818910 PINNACLE MTL INS NEUT36IDX50OD 06/17/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 03/26/2019
-
-