• 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 
 > 
 
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
BETTER BRACES TENS UNIT 08/12/2023
UNKNOWN UNKNOWN TENS UNIT 08/12/2023
UNKNOWN UNKNOWN TENS UNIT 08/12/2023
RST SANEXAS NEOGEN SERIES 10/05/2021
SHENZHEN HONGQIANGXING / SHENZHEN OSTO T BELIFU DUAL CHANNEL TENS EMS UNIT 24 MOD 12/10/2020
SHENZHEN HUAYAN E-COMMERCE CO.,/SHENZHEN BELIFU DUAL CHANNEL TENS EMS UNIT 24 MOD 12/08/2020
BIOMEDICAL LIFE SYSTEMS INC. BIOSTIM SD 03/16/2020
HILL IFC HILL IFC 03/12/2020
HONG QIANGXING (SHEN ZHEN) ELECTRONICS L BELIFU 02/10/2020
ELECTROMEDICAL PRODUCTS INT'L ALPHA-STIM 10/31/2019
-
-