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 
 > 
 
19 records meeting your search criteria returned- Product Code: MDM Product Problem: Bent Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX INC. PARTIAL ECLIPSE DRILL GUIDE/SIZER 05/17/2018
ARTHREX INC. DRIVER SHAFT, T-15, MEDIUM 05/10/2018
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 04/18/2018
ARTHREX, INC. SUREFIRE SCORPION NEEDLE 04/18/2018
ARTHREX INC. SCORPION NEEDLE, KNEE 01/10/2018
ARTHREX, INC. DISPS KIT,TRANS-TIB ACL W/O SAWBLD 07/14/2017
BIOMET TRAUMA RADIOLUCENT TARGETING DEVICE WITH MODULA 04/13/2017
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 04/05/2016
ARTHREX, INC. MULTIFIRE SCORPION NEEDLE 04/05/2016
BIOMET ORTHOPEDICS CINCH HEAD PUSHER/IMPACTOR 01/12/2016
-
-