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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
62 records meeting your search criteria returned- Product Code: GET Product Problem: Failure to Align Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
US SURGICAL PUERTO RICO ENDO DISSECT 02/06/2018
US SURGICAL PUERTO RICO ENDO DISSECT 01/30/2018
US SURGICAL PUERTO RICO ENDO DISSECT 01/16/2018
US SURGICAL PUERTO RICO ENDO DISSECT 01/03/2018
US SURGICAL PUERTO RICO ENDO DISSECT 12/21/2017
US SURGICAL PUERTO RICO ENDO DISSECT 12/01/2017
US SURGICAL PUERTO RICO ENDO DISSECT 06/07/2017
US SURGICAL PUERTO RICO ENDO DISSECT 04/12/2017
COVIDIEN, FORMERLY USSC PUERTO RICO INC ENDO DISSECT* 5MM INSTRUMENT 02/06/2017
COVIDIEN, FORMERLY USSC PUERTO RICO INC ENDO DISSECT* 5MM INSTRUMENT 01/30/2017
-
-