• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
372 records meeting your search criteria returned- Product Code: JEY Patient Problem: Failure of Implant Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SYNTHES GMBH 2.0MM TI MATRIXMANDIBLE SCREW FINE PITCH 02/21/2023
SYNTHES GMBH TI MATRIXMANDIBLE 20 HOLE ADAPTION PL 1. 01/30/2023
SYNTHES GMBH MATRXMND MINI PL-TNSN BND NR3X3H/MAL/1.0 01/30/2023
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
SYNTHES GMBH MATRIXMANDIBLE MINI PL-TENSION BAND BRD/ 01/20/2023
SYNTHES GMBH MATMIDF L-PL 2+3HO R T0.5 TI 01/09/2023
SYNTHES GMBH MATMIDF L-PL 2+3HO LE T0.5 TI 01/09/2023
-
-