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 
 7 
 8 
 9 
 10 
 > 
 
187 records meeting your search criteria returned- Product Code: NIP Product Problem: Entrapment of Device Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION INNOVA VASCULAR 04/29/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 04/23/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 04/14/2021
ABBOTT VASCULAR ABSOLUTE PRO LL SELF-EXPANDING STENT SYS 04/01/2021
BOSTON SCIENTIFIC CORPORATION INNOVA VASCULAR 03/25/2021
ABBOTT VASCULAR ABSOLUTE PRO LL SELF-EXPANDING STENT SYS 03/16/2021
ABBOTT VASCULAR ABSOLUTE PRO LL SELF-EXPANDING STENT SYS 03/01/2021
BOSTON SCIENTIFIC CORPORATION INNOVA VASCULAR 01/04/2021
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT VASCULAR STENT 12/23/2020
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT 5F VASCULAR STENT SYSTEM 10/22/2020
-
-