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

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 
 > 
 
58 records meeting your search criteria returned- Product Code: LZD Patient Problem: Failure of Implant Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TMJ SOLUTIONS, LLC. PATIENT-FITTED TMJ LEFT FOSSA COMPONENT 08/26/2021
BIOMET MICROFIXATION 55MM LFT STANDARD MAND 08/13/2021
BIOMET MICROFIXATION 1479157 PM-TMJ & MODEL 07/19/2021
BIOMET MICROFIXATION LETHBRIDGE PM-TMJ & MODEL 07/12/2021
TMJ SOLUTIONS, LLC. PATIENT-FITTED TMJ RIGHT FOSSA COMPONENT 05/25/2021
TMJ SOLUTIONS, LLC. PATIENT-FITTED TMJ LEFT FOSSA COMPONENT 05/25/2021
BIOMET MICROFIXATION VAQUERO RIGHT PM-TMJ & MODEL 02/23/2021
BIOMET MICROFIXATION TMJ SYSTEM LEFT STANDARD OFFSET MANDIBUL 02/18/2021
BIOMET MICROFIXATION TMJ SYSTEM LEFT FOSSA COMPONENT, SMALL 02/18/2021
TMJ SOLUTIONS, INC. PATIENT-FITTED TMJ LEFT FOSSA COMPONENT 10/07/2020
-
-