• 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 
 > 
 
22 records meeting your search criteria returned- Product Code: ODE Patient Problem: Perforation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENDOGASTRIC SOLUTIONS, INC ESOPHYX Z+ 08/12/2022
ENDOGASTRIC SOLUTIONS, INC ESOPHYX Z+ 07/06/2022
ENDOGASTRIC SOLUTIONS, INC ESOPHYX Z+ 06/27/2022
ENDOGASTRIC SOLUTIONS, INC ESOPHYX Z+ 12/01/2021
ENDOGASTRIC SOLUTIONS, INC ESOPHYX 11/11/2021
ENDOGASTRIC SOLUTIONS, INC ESOPHYX 07/20/2021
ENDOGASTRIC SOLUTIONS, INC ESOPHYX 05/19/2021
ENDOGASTRIC SOLUTIONS, INC ESOPHYX Z+ 05/14/2021
ENDOGASTRIC SOLUTIONS, INC ESOPHYX 05/11/2021
ENDOGASTRIC SOLUTIONS, INC. ESOPHYX2 HD 05/08/2018
-
-