• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
116 records meeting your search criteria returned- Product Code: OAT Patient Problem: Fibrosis Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 03/25/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 03/11/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 03/08/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 03/04/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 02/17/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 01/15/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 01/04/2021
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 12/18/2020
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 12/14/2020
INSTITUT STRAUMANN AG PALATAL IMPLANT 4.1, L 4.2MM 12/11/2020
-
-