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
 

 
 
9 records meeting your search criteria returned- Product Code: JEY Patient Problem: Ossification Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 02/13/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 02/06/2020
BIOMET MICROFIXATION 2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIV 02/06/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 02/06/2020
BIOMET MICROFIXATION 2.4MM SYSTEM HIGH TORQUE (HT) CROSS-DRIV 02/06/2020
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 11/22/2019
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE FOSSA SCREW 11/22/2019
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA S 11/22/2019
BIOMET MICROFIXATION TMJ SYSTEM CROSS DRIVE EMERGENCY FOSSA S 11/22/2019
-
-