• 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 
 > 
 
28 records meeting your search criteria returned- Product Code: OWO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INTERSECT ENT, INC. PROPEL MINI (MOMETASONE FUROATE IMPLANT, 11/14/2020
INTERSECT ENT INC. PROPEL CONTOUR SINUS IMPLANT 10/22/2020
INTERSECT ENT PROPEL SINUS IMPLANT 12/04/2019
INTERSECT ENT PROPEL SINUS IMPLANT 12/04/2019
INTERSECT ENT PROPEL SINUS IMPLANT 12/04/2019
INTERSECT ENT PROPEL SINUS IMPLANT 12/04/2019
INTERSECT ENT PROPEL CONTOUR SINUS IMPLANT 07/17/2018
INTERSECT ENT PROPEL MINI SINUS IMPLANT 07/17/2018
INTERSECT ENT PROPEL CONTOUR SINUS IMPLANT 07/17/2018
INTERSECT ENT PROPEL MINI SINUS IMPLANT 07/17/2018
-
-