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

Manufacturer and User Facility Device Experience(MAUDE)
  • 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 
 > 
 
411 records meeting your search criteria returned- Product Code: JWH Product Problem: Use of Device Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. PERSONA CEMENTED TIBIA 08/28/2024
DEPUY INTERNATIONAL LTD - 8010379 UNK ATTUNE KNEE TIBIAL TRAY 08/27/2024
DEPUY ORTHOPAEDICS INC US UNK KNEE TIBIAL TRAY SIGMA 08/27/2024
DEPUY ORTHOPAEDICS INC US UNK KNEE FEMORAL SIGMA 08/27/2024
DEPUY INTERNATIONAL LTD - 8010379 UNK ATTUNE FEMORAL 08/27/2024
DEPUY IRELAND - 9616671 UNK KNEE FEMORAL ATTUNE PS 08/20/2024
DEPUY IRELAND - 9616671 UNK KNEE TIBIAL TRAY ATTUNE RP 08/20/2024
ZIMMER BIOMET, INC. CRUCIATE RETAINING LEFT SIZE 11 PPS STAN 07/24/2024
DEPUY ORTHOPAEDICS INC US SROM NRH FEM W/PIN XSMRT 66X58 07/18/2024
ZIMMER BIOMET, INC. UNKNOWN PERSONA FEMUR 07/10/2024
-
-