• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
176 records meeting your search criteria returned- Product Code: GEI Product Problem: Loss of or Failure to Bond Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 11/21/2019
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 11/21/2019
DEPUY MITEK LLC US VAPR PREMIERE50 ELECTRODE -EA 11/20/2019
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 11/20/2019
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 11/20/2019
DEPUY MITEK LLC US VAPR VUE GENERATOR 11/20/2019
DEPUY MITEK LLC US VAPR CLPLSE90 ELECTRODE W HAND CNTRLS 11/19/2019
DEPUY MITEK LLC US VAPR P50 W/ HAND CONTROLS 11/19/2019
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 11/19/2019
DEPUY MITEK LLC US VAPR TRIPOLAR 90 SUCTION ELECT 11/19/2019
-
-