• 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 
 > 
 
28 records meeting your search criteria returned- Product Code: KRR 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
ZIMMER BIOMET, INC. FEMORAL COMPONENT 02/20/2024
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 12/26/2023
MEDACTA INTERNATIONAL SA MOTO PARTIAL KNEE PATELLO FEMORAL JOINT 12/21/2023
ZIMMER BIOMET, INC. NEXGEN® COMPLETE KNEE SOLUTION, TRABECU 08/23/2023
ZIMMER BIOMET, INC. RIGHT SIZE 2 PRECOAT CEMENTED PATELLO-FE 08/23/2023
ARTHROSURFACE, INC. HEMICAP PATELLO-FEMORAL RESURFACING PROS 08/11/2020
SMITH & NEPHEW, INC. JOURNEY PF IMPLANT MED LT 06/19/2020
ARTHROSURFACE, INC. HEMICAP PATELLO-FEMORAL RESURFACING PROS 11/04/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN KNEE PATELLA 09/18/2019
ARTHREX, INC. IBALANCE PATELLA IMPLANT DOME, 30 X 8 MM 11/29/2018
-
-