• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 
 
87 records meeting your search criteria returned- Product Code: GZJ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SHENZHEN DONGDIXIN TECHNOTOLOGY CO., LTD INTENSITY CX4 W/ THERAPY CART 03/08/2016
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 DIGITAL TENS 01/05/2016
SHENZHEN DONGDIXIN TECHNOLOGY CO, LTD. INTENSITY 10 11/16/2015
SHENZHEN DONGDIXIN TECHNOLOGY CO., LTD. INTENSITY 10 DIGITAL TENS 05/12/2015
SHENZHEN DONGDIXIN TECHNOLOGY CO., LTD. INTENSITY SELECT COMBO - TENS/IF/MIC/EMS 05/12/2015
EMPI, INC SELECT 1.5 12/12/2014
EMPI, INC SELECT 1.5 10/03/2014
-
-