• 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 
 > 
 
110 records meeting your search criteria returned- Product Code: HRY Patient Problem: Ambulation Difficulties Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. UNK OXFORD BEARING 06/27/2023
ZIMMER BIOMET, INC. VAN PS OPEN INTL FEM-LT 67.5 09/24/2022
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 05/31/2022
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 05/31/2022
BIOMET UK LTD. UNKNOWN OXFORD BEARING 05/31/2022
MICROPORT ORTHOPEDICS INC. EVOLUTION® MP? CS INSERT SIZE 5+ 10MM LE 09/23/2021
ZIMMER BIOMET, INC. VNGD TI FEM CR 62.5MM RT 07/23/2021
SMITH & NEPHEW, INC. UNKN LEGION TOTAL KNEE REV FEM COMP 07/14/2021
BIOMET UK LTD. UNKNOWN OXFORD FEMORAL COMPONENT 02/24/2021
AESCULAP AG COLLECT.NO.QAS KNEE IMPL.VEGA 01/08/2021
-
-