• 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 
 > 
 
34 records meeting your search criteria returned- Product Code: MFR Patient Problem: Complaint, Ill-Defined Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR 09/14/2020
MEDTRONIC NEUROMODULATION KINETRA 12/07/2017
MEDTRONIC NEUROMODULATION UNKNOWN IMPLANTABLE NEUROSTIMULATOR 07/10/2017
MEDTRONIC NEUROMODULATION unknown brand name 12/16/2016
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 12/12/2016
MEDTRONIC MED REL MEDTRONIC PUERTO RICO ACTIVA 12/12/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. RECLAIM 12/06/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 11/17/2016
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 11/17/2016
MEDTRONIC NEUROMODULATION UNKNOWN DEEP BRAIN NEUROSTIMULATOR 10/28/2016
-
-