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

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 records meeting your search criteria returned- Product Code: GET Product Problem: Defective Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LINVATEC CORPORATION D/B/A CONMED LINVAT HALL SURGAIRTOME 09/07/2018
IMT AG / INTEGRATED MEDICAL TECHNOLOGIES WOODPECKER, TOTAL HIP BROACHING SYSTEM 08/08/2017
AESCULAP AG & CO. KG AIR HOSE 5.0M AESC. -DRAEGER/AESC.LARGE 08/13/2015
COVIDIEN, FORMERLY USSC PUERTO RICO INC ROTICULATOR ENDO GRASP* 5MM W/SPIN LOCK 04/07/2015
-
-