• 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 
 > 
 
29 records meeting your search criteria returned- Product Code: HRY Patient Problem: Synovitis Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. VNGD CR TIB BRG 10X63/67 10/05/2023
BIOMET UK LTD. UNK OXFORD BEARING 06/27/2023
BIOMET UK LTD. RHK 12X80 CEMENTED STEM 08/30/2022
BIOMET UK LTD. UNKNOWN TIBIAL TRAY 09/21/2021
BIOMET UK LTD. UNKNOWN BEARING 09/21/2021
AESCULAP AG AS VEGA PS FEMORAL COMP.CEMENTED F6N R 01/05/2021
AESCULAP AG VEGA PS GLIDING SURFACE T3/3+ 14MM 01/05/2021
AESCULAP AG PATELLA 3-PEGS P4 01/05/2021
AESCULAP AG PLUG F/TIBIAL PLATEAU 01/05/2021
AESCULAP AG AS VEGA PS TIBIAL PLATEAU CEMENTED T3 01/05/2021
-
-