• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
148 records meeting your search criteria returned- Product Code: LZD Patient Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD MANDIBULAR COM 09/13/2022
BIOMET MICROFIXATION TMJ SYSTEM RIGHT FOSSA COMPONENT, SMALL 09/13/2022
BIOMET MICROFIXATION UNKNOWN LEFT TMJ MANDIBLE COMPONENT 09/13/2022
BIOMET MICROFIXATION UNKNOWN LEFT TMJ FOSSA COMPONENT 09/13/2022
BIOMET MICROFIXATION TMJ SYSTEM SMALL RIGHT FOSSA COMPONENT 09/06/2022
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD MANDIBULAR COM 09/06/2022
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 09/01/2022
BIOMET MICROFIXATION UNKNOWN LEFT FOSSA 08/30/2022
BIOMET MICROFIXATION UNKNOWN LEFT MANDIBLE 08/30/2022
BIOMET MICROFIXATION UNKNOWN RIGH FOSSA 08/30/2022
-
-