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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
249 records meeting your search criteria returned- Product Code: LWJ Product Problem: Fracture Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 28MM S 09/20/2019
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 28MM S 08/02/2019
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 06/26/2019
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 06/07/2019
DEPUY FRANCE SAS - 3003895575 CORAIL REVISION STEM HO 13 04/24/2019
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 28MM S 02/06/2019
SMITH & NEPHEW ORTHOPAEDICS AG UNKNOWN SMITH AND NEPHEW POLYETHYLENE IN 01/29/2019
CORIN MEDICAL TRINITY 12/14/2018
ZIMMER BIOMET, INC. ZMR FEMORAL STEM REVISION TAPER 12/11/2018
AESCULAP AG BIOLOX PROSTHESIS HEAD 12/14 32MM S 10/31/2018
-
-