• 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 
 7 
 > 
 
64 records meeting your search criteria returned- Product Code: HWT Product Problem: Unintended Movement Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 06/21/2022
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 06/21/2022
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 06/21/2022
DEPUY IRELAND - 9616671 ATTUNE MES SIZING/ROT GDE 06/15/2022
DEPUY ORTHOPAEDICS INC US UNK FEMORAL TRIAL 05/31/2022
DEPUY IRELAND - 9616671 SIG HP REV TC3 BOX TRIAL SZ4 05/07/2022
DEPUY IRELAND - 9616671 ATTUNE SPACER BLOCK 03/23/2022
DEPUY ORTHOPAEDICS INC US ARTIC/EZE TR BALL GRVD 32+5 02/14/2022
DEPUY IRELAND - 9616671 ATTUNE DISTAL FEMORAL JIG 02/01/2022
DEPUY IRELAND - 9616671 ATTUNE DISTAL FEMORAL JIG 12/07/2021
-
-