• 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 
 > 
 
40 records meeting your search criteria returned- Product Code: NIQ Patient Problem: Pain Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 03/17/2022
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 02/23/2022
ABBOTT VASCULAR XIENCE EVEROLIMUS ELUTING CORONARY STENT 02/09/2022
ABBOTT VASCULAR XIENCE XPEDITION 48 EVEROLIMUS ELUTING C 02/04/2022
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 10/13/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY 05/20/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 05/13/2021
BOSTON SCIENTIFIC CORPORATION PROMUS ELEMENT PLUS 03/22/2021
BOSTON SCIENTIFIC CORPORATION PROMUS PREMIER 11/02/2020
ABBOTT VASCULAR XIENCE SIERRA EVEROLIMUS ELUTING CORONAR 06/29/2020
-
-