• 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 
 > 
 
491 records meeting your search criteria returned- Product Code: NRY Product Problem: Fracture Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER NEUROVASCULAR CORK AXS CATALYST 7 .068IN ID X 132CM - US 03/06/2024
NEURAVI LTD. EMBOTRAP III 6.5 MM X 45 MM 03/05/2024
PENUMBRA, INC. PENUMBRA SYSTEM RED 72 REPERFUSION CATHE 02/23/2024
PENUMBRA, INC. PENUMBRA SYSTEM ACE 60 REPERFUSION CATHE 02/22/2024
STRYKER NEUROVASCULAR-CALIF AXS VECTA 071 CATH 132CM - US 02/14/2024
PENUMBRA, INC. PENUMBRA SYSTEM JET7 REPERFUSION CATHETE 02/13/2024
PENUMBRA, INC. PENUMBRA SYSTEM JET7 REPERFUSION CATHETE 02/05/2024
STRYKER NEUROVASCULAR CORK AXS CATALYST 7 .068IN ID X 132CM - CE 01/29/2024
STRYKER NEUROVASCULAR-UTAH-SALT LAKE CIT TREVO XP PROVUE 4MM X 30MM 01/16/2024
MICROVENTION, INC. ERIC 6 01/12/2024
-
-