• 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 
 > 
 
307 records meeting your search criteria returned- Product Code: KWY Patient Problem: Not Applicable Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP IMPLANT 09/17/2018
DEPUY ORTHOPAEDICS INC 1818910 UNKNOWN HIP FEMORAL STEM 09/17/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL HEAD 09/17/2018
DEPUY INTERNATIONAL LTD - 8010379 P.F.C.* 28MM HEAD +0MM 09/13/2018
DEPUY ORTHOPAEDIC INC, 1818910 UNKNOWN OTHER PRODUCTS 09/12/2018
DEPUY ORTHOPAEDICS, INC. 1818910  SELF CENT HIP 40X28 RUST 09/12/2018
DEPUY ORTHOPAEDICS, INC. 1818910  UNKNOWN HIP FEMORAL STEM 09/12/2018
CORENTEC CO., LTD. BENCOX TOTAL HIP SYSTEM INSTRUMENT HEAD 09/11/2018
DEPUY INTERNATIONAL LTD. 8010379 UNKNOWN HIP FEMORAL AUGMENT 09/10/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP ACETABULAR LINERS 09/10/2018
-
-