• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN 03/10/2020
MPRI CAPSUREFIX NOVUS MRI SURESCAN 03/06/2020
MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN 01/29/2020
BOSTON SCIENTIFIC CORPORATION FINELINE II STEROX 01/10/2020
BOSTON SCIENTIFIC CORPORATION FINELINE II EZ STEROX 01/06/2020
MICROPORT CRM S.R.L. ENO 01/03/2020
MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN 12/12/2019
MPRI CAPSUREFIX NOVUS LEAD MRI SURESCAN 11/18/2019
MPRI CAPSUREFIX NOVUS MRI SURESCAN 11/07/2019
BOSTON SCIENTIFIC CORPORATION FLEXTEND 2 11/02/2019
-
-