• 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 
 > 
 
61 records meeting your search criteria returned- Product Code: KWY Product Problem: Nonstandard Device Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY INTERNATIONAL LTD - 8010379 UNK HIP FEMORAL SLEEVE ASR 11/20/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/16/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL HEAD 09/30/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL AUGMENT 09/28/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL HEAD 09/03/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL AUGMENT 07/17/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL AUGMENT 06/04/2020
DEPUY INTERNATIONAL LTD - 8010379 UNK HIP FEMORAL SLEEVE ASR 05/21/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL AUGMENT 05/20/2020
DEPUY INTERNATIONAL LTD - 8010379 UNKNOWN HIP FEMORAL HEAD 04/22/2020
-
-