• 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 PUERTO RICO OPERATIONS CO. INTELLIS 07/15/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SURESCAN 07/01/2020
BOSTON SCIENTIFIC NEUROMODULATION unknown brand name 06/18/2020
BOSTON SCIENTIFIC NEUROMODULATION unknown brand name 06/17/2020
ST. JUDE MEDICAL - NEUROMODULATION PENTA 3MM LEAD, 60 CM 06/12/2020
ST. JUDE MEDICAL - NEUROMODULATION EXCLAIM LEAD, 90 CM 06/09/2020
MEDTRONIC PUERTO RICO OPERATIONS CO. SURESCAN 05/22/2020
MEDTRONIC NEUROMODULATION SPINAL-CORD STIMULATOR 05/06/2020
BOSTON SCIENTIFIC NEUROMODULATION PRECISION 04/22/2020
BOSTON SCIENTIFIC NEUROMODULATION PRECISION 04/06/2020
-
-