• 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 
 > 
 
17 records meeting your search criteria returned- Product Code: JEY Product Problem: Noise, Audible Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION 1.5/0.6 2MM LEFORT PLATE 11/29/2023
BIOMET MICROFIXATION 1.5/0.6 2MM LEFORT PLATE 11/29/2023
BIOMET MICROFIXATION 2.0/1.0 4 HOLE REG 05/26/2021
BIOMET MICROFIXATION 2.0/1.0 4 HOLE REG 05/26/2021
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA S 11/03/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 2.0MM 11/03/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 01/03/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA S 02/06/2019
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 2.0 X 02/06/2019
BIOMET MICROFIXATION TMJ SYSTEM CROSS-DRIVE FOSSA SCREW, 2.0 01/04/2019
-
-