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
 

 
 
 1 
 2 
 > 
 
15 records meeting your search criteria returned- Product Code: LXH Patient Problem: Perforation of Vessels Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH ROUND DISK 11/04/2022
SYNTHES GMBH ROUND DISK 11/04/2022
EIT EMERGING IMPLANT TECHNOLOGIES GMBH SHAVER H 9MM 09/26/2022
STRYKER GMBH UNKNOWN DRILL 09/15/2022
STRYKER SPINE-US UNKNOWN INSTRUMENT 09/15/2021
NUVASIVE INC. NUVASIVE GENERAL INSTRUMENTS 06/10/2020
STRYKER TRAUMA KIEL TARGET DEVICE, HUMERUS T2 HUMERUS 10/26/2018
ZIMMER BIOMET, INC. UNKNOWN INSTRUMENT 04/18/2018
SPINEOLOGY INC. ARTICULATING CURETTE 03/30/2017
MEDTRONIC SOFAMOR DANEK USA, INC ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 12/02/2016
-
-