• 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 
 > 
 
29 records meeting your search criteria returned- Product Code: LZD Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET MICROFIXATION UNKNOWN LEFT FOSSA 02/07/2023
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 09/01/2022
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 07/21/2022
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 12/28/2021
BIOMET MICROFIXATION 6616575 PM-TMJ & MODEL 03/16/2021
BIOMET MICROFIXATION CUSTOM MADE DEVICE FISHER PM-TMJ & MODEL 12/13/2020
BIOMET MICROFIXATION NAIDOO PM-TMJ & MODEL 07/20/2020
BIOMET MICROFIXATION CUSTOM MADE DEVICE COENEN PM-TMJ & MODEL 02/18/2020
BIOMET MICROFIXATION CUSTOM MADE DEVICE 12/05/2019
BIOMET MICROFIXATION TMJ SYSTEM RIGHT STANDARD OFFSET MANDIBU 11/22/2019
-
-