• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
482 records meeting your search criteria returned- Product Code: LXH Product Problem: Bent Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER GMBH UNKNOWN AXSOS 3 5,0MM PLATE 01/19/2018
DEPUY ORTHOPAEDICS INC US PIN TRL LNR 10DEG +4 40ID 58OD 01/12/2018
STRYKER SPINE-FRANCE RELIANCE AL DISCECTOMY DISTRACTOR 01/10/2018
ZIMMER BIOMET, INC. SCANDIMED OPTIGUN 01/09/2018
DEPUY ORTHOPAEDICS INC US UNKNOWN OTHER PRODUCTS 01/08/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC 3.2MM GUIDE WIRE 400MM 01/05/2018
K2M INC. EVEREST SPINAL SYSTEM 01/05/2018
DEPUY ORTHOPAEDICS, INC. 1818910 EXCEL T-HANDLE 01/05/2018
DEPUY ORTHOPAEDICS INC US PIN TRL LNR NEUT 560DX36ID 01/04/2018
DEPUY MITEK EXPRESSEW III NEEDLE PK5 12/28/2017
-
-