• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
209 records meeting your search criteria returned- Product Code: GZB Product Problem: Inappropriate/Inadequate Shock/Stimulation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STIMWAVE TECHNOLOGIES INC. FREEDOM NEUROSTIMULATOR 03/10/2021
STIMWAVE TECHNOLOGIES INC. FREEDOM NEUROSTIMULATOR 03/10/2021
STIMWAVE TECHNOLOGIES INC. FREEDOM NEUROSTIMULATOR 03/10/2021
STIMWAVE TECHNOLOGIES INC FREEDOM NEUROSTIMULATOR 12/25/2020
STIMWAVE TECHNOLOGIES, INC. STIMWAVE 01/22/2020
ST. JUDE MEDICAL - NEUROMODULATION EXTENSION, DUAL 4 CHANNEL 10CM 09/24/2019
ST. JUDE MEDICAL - NEUROMODULATION EXTENSION, DUAL 4 CHANNEL 10CM 09/24/2019
ABBOTT MEDICAL PENTA LEAD 03/19/2019
ST JUDE MEDICAL / ABBOTT LABORATORIES NEUROSTIMULATION SYSTEM 08/24/2018
MEDTRONIC INC. MEDTRONIC RESTORE ULTRA 37712 05/09/2018
-
-