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 
 
 
11 records meeting your search criteria returned- Product Code: LZD Patient Problem: Inadequate Osseointegration Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS UNKNOWN_FRO_PRODUCT 03/28/2024
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS UNKNOWN_FRO_PRODUCT 03/12/2024
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS UNKNOWN_CMF_PRODUCT 01/19/2024
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BONE SCREW 2.0MM X 6MM 06/21/2023
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS UNKNOWN_FRO_PRODUCT 06/06/2023
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 03/07/2023
TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS TMJ BILATERAL IMPLANTS 08/03/2022
TMJ SOLUTIONS, LLC. PATIENT-FITTED TMJ RIGHT MANDIBULAR COMP 07/13/2021
TMJ SOLUTIONS, LLC. PATIENT-FITTED TMJ RIGHT MANDIBULAR COMP 06/02/2021
TMJ SOLUTIONS, INC. PATIENT-FITTED TMJ RIGHT MANDIBULAR COMP 12/10/2020
-
-