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

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 
 4 
 5 
 > 
 
46 records meeting your search criteria returned- Product Code: OCW Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN ENDO STITCH 02/23/2016
COVIDIEN ENDOSTITCH 02/17/2016
COVIDIEN ENDO STITCH 11/19/2015
COVIDIEN, FORMERLY US SURGICAL A DIVISON SILS STITCH SUTURING DEVICE 09/29/2015
COVIDIEN, FORMERLY US SURGICAL A DIVISON SILS STITCH SUTURING DEVICE 09/29/2015
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 09/01/2015
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 08/25/2015
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 08/25/2015
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 08/21/2015
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 08/20/2015
-
-