• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
292 records meeting your search criteria returned- Product Code: JWH Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ATTUNE PS FEM RT SZ 7 CEM 01/23/2020
SMITH & NEPHEW, INC. KNEE IMPLANT 01/13/2020
DEPUY IRELAND - 9616671 ATTUNE PS FEM RT SZ 9 CEM 01/09/2020
DEPUY ORTHOPAEDICS INC US UNIVERSAL STEM 75X14MM FLUTED 01/06/2020
DEPUY ORTHOPAEDICS INC US UNIVERSAL STEM 75X14MM FLUTED 01/06/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE FEMORAL SLEEVE 12/27/2019
UNKNOWN REPLACEMENT HIP 12/23/2019
UNKNOWN KNEE 12/23/2019
SMITH & NEPHEW, INC. LGN PS HIGH FLEX XLPE SZ 5-6 9MM 12/15/2019
SMITH & NEPHEW, INC. KNEE IMPLANT 12/15/2019
-
-