• 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 
 3 
 4 
 5 
 6 
 7 
 > 
 
65 records meeting your search criteria returned- Product Code: JEY Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION UNKNOWN SCREW 03/20/2023
STRYKER LEIBINGER FREIBURG BONE SCREW,AXS,SD,1.7X6MM,5P 02/28/2023
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA S 01/25/2023
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 01/25/2023
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 01/25/2023
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 01/25/2023
KARL LEIBINGER MEDIZINTECHNIK GMBH & CO. LEVEL ONE CMF 11/23/2022
MATERIALISE NV TRUMATCH 09/29/2022
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 2.0MM 09/25/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 2.0MM 09/25/2020
-
-