• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: HXI Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. GUIDE WIRE GRIPPER 11/13/2018
ZIMMER BIOMET, INC. GUIDE WIRE GRIPPER 08/22/2018
ZIMMER BIOMET, INC. ZNN GUIDE WIRE GRIPPER 08/02/2018
ZIMMER BIOMET, INC. ZNN GUIDE WIRE GRIPPER 06/13/2018
ZIMMER BIOMET, INC. ZNN GUIDE WIRE GRIPPER 06/13/2018
ASCENSION ORTHOPEDICS 3.0 / 4.0 SMOOTH K-WIRE 03/15/2018
ZIMMER BIOMET, INC. ZIMMER NATURAL NAIL GUIDE WIRE GRIPPER 09/29/2017
ZIMMER BIOMET, INC. ZIMMER NATURAL NAIL GUIDE WIRE GRIPPER 09/29/2017
ZIMMER BIOMET, INC. ZNN GUIDE WIRE GRIPPER 09/13/2017
ZIMMER, INC. ZIMMER ZNN GUIDE WIRE GRIPPER 10/14/2016
-
-