• 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 
 8 
 9 
 10 
 > 
 
93 records meeting your search criteria returned- Product Code: KWL Product Problem: Loss of Osseointegration Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 6 10/30/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 6 09/11/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 10 09/11/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 6 09/10/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED STD SIZE 7 07/13/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 6 06/24/2020
DEPUY ORTHOPAEDICS INC US ACTIS COLLARED STD SIZE 3 04/08/2020
STRYKER ORTHOPAEDICS-MAHWAH ODC CEMENTED HIP #6 132 04/02/2020
DEPUY ORTHOPAEDICS INC US TRI-LOCK TI 11.3 STD OFFSET 03/18/2020
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 10 03/06/2020
-
-