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

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: KWY Product Problem: Unintended Movement Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER SWITZERLAND MANUFACTURER GMBH BIPOLAR INSERT, MODULAR, 42/28 06/20/2023
BIOMET UK LTD. UNKNOWN CEMENTED UKR 12/07/2020
BIOMET UK LTD. UNKNOWN CERAMIC HEAD 11/17/2020
BIOMET UK LTD. UNKNOWN EXCEED ABT CERAMIC LINER 11/17/2020
BIOMET UK LTD. UNKNOWN EXCEED ABT CERAMIC LINER 11/17/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 10/07/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/12/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/12/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/12/2020
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL STEM 06/12/2020
-
-