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 
 
 
11 records meeting your search criteria returned- Product Code: NRY Product Problem: Premature Separation Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NEURAVI LTD. EMBOTRAP III 6.5 MM X 45 MM 09/05/2023
NEURAVI LTD. EMBOTRAP II 5X33 REVASC. DEV. 03/22/2023
NEURAVI LTD. EMBOTRAP III 6.5 MM X 45 MM 06/07/2022
NEURAVI LTD. EMBOTRAP II 5X21 REVASC. DEV. 04/20/2021
NEURAVI LTD. EMBOTRAP II 5X33 REVASC. DEV. 02/11/2021
NEURAVI LTD. EMBOTRAP II 5X33 REVASC. DEV. 12/08/2020
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 08/05/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 07/12/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 06/05/2019
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 05/30/2019
-
-