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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
444 records meeting your search criteria returned- Product Code: HSX Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL L.P EMPOWR PARTIAL KNEETM, TIBIAL INSERT, SI 09/05/2023
SMITH & NEPHEW, INC. ENGAGE POROUS FEMORAL SZ 7-LT MED 09/05/2023
ENCORE MEDICAL L.P EMPOWR PARTIAL KNEETM, TIBIAL INSERT, SI 08/28/2023
ZIMMER BIOMET, INC. ZIMMER UNICOMPARTMENTAL ARTICULAR SURFAC 08/25/2023
SMITH & NEPHEW, INC. ENGAGE POROUS FEMORAL SZ 4-RT MED 08/17/2023
MEDACTA INTERNATIONAL SA MOTO PARTIAL KNEE ANATOMICAL FEMORAL COM 08/10/2023
SMITH & NEPHEW, INC. JOURNEY II UK TIB INSRT MED SZ 7-8 8MM 07/20/2023
ENCORE MEDICAL L.P EMPOWR PARTIAL KNEETM, FEMUR, NP, SIZE 5 07/20/2023
ENCORE MEDICAL L.P EMPOWR PARTIAL KNEETM, FEMUR, NP, SIZE 5 07/17/2023
ZIMMER BIOMET, INC. UNKNOWN ZIMMER UNICOMPARTMENTAL KNEE FEM 06/06/2023
-
-