• 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 
 > 
 
216 records meeting your search criteria returned- Product Code: LWJ Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 11/07/2023
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 09/19/2023
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 11/07/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 11/07/2022
CORIN MEDICAL TRINITY 10/10/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 08/10/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® R GRIT BLASTED PROX BODY SMALL 07/19/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® ROUGHENED DISTAL STEM, TAPERED 07/19/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 04/01/2022
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 10/13/2021
-
-