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

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 
 > 
 
14 records meeting your search criteria returned- Product Code: NRY Product Problem: Bent Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 06/11/2018
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 HI-FLOW KIT 04/06/2018
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 03/13/2018
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 03/12/2018
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 REPERFUSION CATHE 01/10/2018
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 09/26/2017
PENUMBRA, INC. PENUMBRA SYSTEM ACE 64 HI-FLOW KIT 04/18/2017
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 HI-FLOW KIT 08/31/2016
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 06/07/2016
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 12/17/2015
-
-