Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
160 records meeting your search criteria returned- Product Code: HRY Patient Problem: Failure of Implant Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKN FEM HEAD MEMPHIS OX 12/09/2021
SMITH & NEPHEW, INC. UNKN JOURNEY BCS KNEE INSERT 11/09/2021
SMITH & NEPHEW, INC. MI TRIAL FEM HEAD 36 -3 11/03/2021
SMITH & NEPHEW, INC. MI TRIAL FEM HEAD 36 +4 11/03/2021
SMITH & NEPHEW, INC. LEGION HK 4.75 HEX TORQUE WRENCH ADAPT 10/12/2021
BIOMET UK LTD. UNKNOWN OXFORD BEARING 09/27/2021
MICROPORT ORTHOPEDICS INC. EVOLUTION® MP? CS INSERT SIZE 5+ 10MM LE 09/23/2021
SMITH & NEPHEW, INC. UNKN JOURNEY KNEE IMPL 07/29/2021
ZIMMER BIOMET, INC. VANGUARD CR LIP TIB BRG 12X63/67 07/26/2021
SMITH & NEPHEW, INC. UNKN JOURNEY BCS / JOURNEY II BCS KNEE I 07/22/2021
-
-