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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
60 records meeting your search criteria returned- Product Code: MHY Product Problem: No Device Output Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC NEUROMODULATION PERCEPT 05/16/2023
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/20/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 10/06/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 09/30/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. PERCEPT 09/07/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 07/05/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 02/28/2022
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 12/20/2021
MEDTRONIC NEUROMODULATION IMPLANTABLE NEUROSTIMULATOR 11/18/2021
MEDTRONIC PUERTO RICO OPERATIONS CO. ACTIVA 06/21/2021
-
-