• 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
 

 
 
8 records meeting your search criteria returned- Product Code: NDP Patient Problem: Osteopenia/ Osteoporosis Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
IMPLANT DIRECT SYBRON MANUFACTURING LLC REPLANT IMPLANT ANALOG 10/18/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC REPLANT IMPLANT ANALOG 10/18/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC SIMPLYLEGACY DRIVER 10/06/2023
IMPLANT DIRECT SYBRON MANUFACTURING LLC LEGACY IMPLANT CLOSED-TRAY TRANSFER 04/27/2022
IMPLANT DIRECT SYBRON MANUFACTURING LLC IMPLANT REMOVAL TOOL 10/04/2021
IMPLANT DIRECT SYBRON MANUFACTURING LLC HEX TOOL 10/22/2020
IMPLANT DIRECT SYBRON MANUFACTURING LLC SIMPLYLEGACY DRIVER 08/13/2020
IMPLANT DIRECT SYBRON MANUFACTURING LLC HEX TOOL 04/24/2019
-
-