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
 

 
 
8 records meeting your search criteria returned- Product Code: MBI Product Problem: Torn Material Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5 10/05/2016
SMITH & NEPHEW, INC. FOOTPRINT ULTRA PK SUTURE ANCHOR, 4.5 12/05/2015
DEPUY MITEK MITEK RIGIDLOOP ADJUSTABLE CORTICAL IMPL 09/16/2015
SMITH & NEPHEW, INC. TF ULTRA PK 5.5MMCOBRD WHTBL COBRD BL BL 09/08/2015
BIOMET ORTHOPEDICS JUGGERKNOT 1.0MM MINI 2-0 NDLS 06/26/2015
ARTHROCARE CORPORATION MULTIFIX P KNOTLESS FIXATION DEVICE 04/06/2015
ARTHROCARE CORPORATION MAGNUM 2 PLUS PERFECTPASSER CONNECTOR MA 04/06/2015
BIOMET ORTHOPEDICS #7 PE ZIPLOOP EXT TOGGLELOC 04/09/2014
-
-