• 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 
 6 
 7 
 > 
 
62 records meeting your search criteria returned- Product Code: MAI Product Problem: Entrapment of Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US GRYPHON P BR W PERMACORD 12/07/2018
DEPUY MITEK LLC US GRYPHON P BR DSW PERMACORD 12/07/2018
DEPUY MITEK LLC US GRYPHON P BR W PERMACORD 12/07/2018
ARTHREX, INC. BIO-COMP INTERFSCRW W/DISP SHTH 11/15/2018
DEPUY MITEK LLC US VERSALOK PEEK WITH ORTHOCORD 10/03/2018
ARTHREX INC. 5.5MM BC CORKSCREW FT W/ SUTURETAPE 04/05/2018
ARTHREX INC. BIO-COMPOSITE INTER-FERENCE SCRW 08/23/2017
ARTHREX, INC. BIO-COMP SWVLK SP, 4.75X24.5MM 10/27/2016
ARTHREX, INC. BIO-COMP. SUTURE TAK 08/16/2016
ARTHREX, INC. SUTURE ANCHOR BIOCOMPOSITE CORKSCREW FT 02/03/2016
-
-