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

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
 

 
 
7 records meeting your search criteria returned- Product Code: LWJ Product Problem: Mechanical Jam Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. PROFEMUR® MODULAR FEMORAL NECK 11/28/2023
CORIN MEDICAL TRINITY 07/14/2021
SMITH & NEPHEW ORTHOPAEDICS AG POLARCUP SHELL TI-PLASMA/HA 45 NON-CEM 06/24/2021
SMITH & NEPHEW ORTHOPAEDICS AG POLARCUP SHELL TI-PLASMA/HA 49 NON-CEM 01/13/2021
CORIN MEDICAL TRINITY 02/21/2020
CORIN MEDICAL TRINITY 08/08/2016
MICROPORT ORTHOPEDICS INC. PROFEMUR(R) MODULAR FEMORAL NECK 08/25/2014
-
-