• 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 
 > 
 
36 records meeting your search criteria returned- Product Code: KWY Patient Problem: Hip Fracture Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET FRANCE S.A.R.L. VARIZED FEMORAL STEM EXCEPTION RIGHT SIZ 12/09/2020
ZIMMER BIOMET, INC. UNKNOWN BI-METRIC STEM 10/29/2020
DEPUY ORTHOPAEDICS, INC. BIPOLAR HIP ASSEMBLY 10/15/2020
SMITH & NEPHEW, INC. UNKN TANDEM BIPOLAR/UNIPOLAR IMPL 10/14/2020
BIOMET FRANCE S.A.R.L. UPTION COMPLETE FEMORAL STEM 09/30/2020
ZIMMER SWITZERLAND MANUFACTURING GMBH ALLOCLASSICA, CSF SHELL, UNCEMENTED, 64 04/07/2020
OMNILIFE SCIENCE, INC. OMNI HIP SYSTEM 07/03/2019
ZIMMER BIOMET, INC. ARCOS CON SZ B STD 60MM HA 08/31/2018
ZIMMER BIOMET, INC. ARCOS 16X190MM SPL TPR DIST HA 08/31/2018
ORTHO DEVELOPMENT PIVOT 08/22/2018
-
-