• 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 
 > 
 
53 records meeting your search criteria returned- Product Code: HWT Product Problem: Use of Device Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ATTUNE FB CR ARTIC SURF SZ4 05/19/2021
DEPUY IRELAND - 9616671 ATTUNE FB CR ARTIC SURF SZ8 05/19/2021
DEPUY IRELAND - 9616671 ATTUNE FB CR ARTIC SURF SZ5 05/19/2021
DEPUY IRELAND - 9616671 ATTUNE SPACER BLOCK 05/19/2021
DEPUY IRELAND - 9616671 ATTUNE SHIM SZ7 6MM 05/03/2021
DEPUY IRELAND - 9616671 ATTUNE SPACER BLOCK 04/08/2021
DEPUY IRELAND - 9616671 ATTUNE SPACER BLOCK 03/23/2021
DEPUY IRELAND - 9616671 ATTUNE RP PS ARTIC SURF SZ6 03/18/2021
DEPUY ORTHOPAEDICS INC US S/C & MOD CATH TRL 50/28 03/15/2021
DEPUY IRELAND - 9616671 ATTUNE RP PS ARTIC SURF SZ5 03/12/2021
-
-