• 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 
 > 
 
412 records meeting your search criteria returned- Product Code: OIY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL L.P. 3D KNEE 10/11/2022
ENCORE MEDICAL L.P. 3D KNEE 10/07/2022
ENCORE MEDICAL L.P. MOVATION KNEE 09/30/2022
ZIMMER BIOMET, INC. FEMUR TRABECULAR METAL CRUCIATE RETAININ 09/14/2022
ENCORE MEDICAL L.P. MOVATION KNEE 09/01/2022
ENCORE MEDICAL L.P. 3D KNEE 09/01/2022
ZIMMER BIOMET, INC. VAN PS OPEN INTL FEM-LT 60 07/06/2022
ZIMMER BIOMET, INC. UNKNOWN ARTICULAR SURFACE 07/06/2022
ZIMMER BIOMET, INC. VANGUARD CR ILOK FEM-RT 06/24/2022
ENCORE MEDICAL L.P MOVATION KNEE 04/29/2022
-
-