• 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 
 > 
 
196 records meeting your search criteria returned- Product Code: LGW Patient Problem: Nerve Damage Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC MED REL MEDTRONIC PUERTO RICO RESTORE SENSOR 10/16/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 09/19/2019
MEDTRONIC NEUROMODULATION STIMULATOR, SPINAL-CORD, TOTALLY IMPLANT 09/03/2019
BOSTON SCIENTIFIC NEUROMODULATION STIMULATOR, SPINAL-CORD, TOTALLY IMPLANT 07/22/2019
MEDTRONIC MED REL MEDTRONIC PUERTO RICO SYNERGY 06/12/2019
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 04/24/2019
MEDTRONIC NEUROMODULATION STIMULATOR, SPINAL-CORD, TOTALLY IMPLANT 04/15/2019
NEVRO CORP. SENZA 04/12/2019
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE TRIAL LEAD KIT, 60CM LENGTH 04/08/2019
ST. JUDE MEDICAL - NEUROMODULATION (PUER OCTRODE TRIAL LEAD KIT, 60CM LENGTH 04/08/2019
-
-