• 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 
 8 
 > 
 
73 records meeting your search criteria returned- Product Code: OCW Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN LP ENDO STITCH 08/07/2019
COVIDIEN ENDOSTITCH SUTURING DEVICE (10MM) 07/30/2019
COVIDIEN ENDO STITCH SUTURING DEVICE 07/22/2019
COVIDIEN LLC ENDO STITCH 10 MM 07/15/2019
COVIDIEN ENDO STITCH 07/12/2019
COVIDIEN LP ENDO STITCH 07/10/2019
COVIDIEN LP ENDO STITCH 07/09/2019
COVIDIEN LP ENDO STITCH 06/19/2019
AESCULAP AG SHAFT COMPL.D:10MM L:370MM 06/06/2019
AESCULAP AG SHAFT COMPL.D:10MM L:370MM 06/06/2019
-
-