• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
256 records meeting your search criteria returned- Product Code: LZD Product Problem: Insufficient Information Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL 05/23/2018
BIOMET MICROFIXATION TMJ SYSTEM LEFT NARROW MANIBULAR COMPONE 05/23/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD OFFSET MANDIBU 05/18/2018
BIOMET MICROFIXATION TMJ SYSTEM LEFT STANDARD MANDIBULAR COMP 05/08/2018
BIOMET MICROFIXATION TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL 05/08/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD OFFSET MANDIBU 05/08/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL 05/08/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT NARROW MANDIBULAR COMPO 05/03/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL 03/26/2018
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD MANDIBULAR COM 03/26/2018
-
-