Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
245 records meeting your search criteria returned- Product Code: LGW Product Problem: Human-Device Interface Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC PUERTO RICO OPERATIONS CO. SURESCAN 08/07/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 07/10/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. SURESCAN 07/03/2018
MEDTRONIC NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR 06/11/2018
MEDTRONIC MED REL MEDTRONIC PUERTO RICO PRIMEADVANCED 05/30/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. RESTORE SENSOR 05/11/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. SURESCAN 04/30/2018
MEDTRONIC PUERTO RICO OPERATIONS CO. INTELLIS 04/30/2018
MEDTRONIC NEUROMODULATION STIMULATOR, SPINAL-CORD, TOTALLY IMPLANT 04/10/2018
MEDTRONIC NEUROMODULATION INTELLIS 03/23/2018
-
-