• 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 
 7 
 8 
 9 
 10 
 > 
 
195 records meeting your search criteria returned- Product Code: NHA Product Problem: Failure to Osseointegrate Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INSTITUT STRAUMANN AG RN HEALING CAP, H 2.0MM, TI 07/12/2024
ZEST ANCHORS, LLC LOCATOR OVERDENTURE IMPLANT SYSTEM (LODI 06/28/2024
BIOHORIZONS INC. BIOHORIZONS INC. 05/17/2024
BIOHORIZONS INC. BIOHORIZONS INC. 04/01/2024
BIOHORIZONS BIOHORIZONS 03/22/2024
BIOHORIZONS BIOHORIZONS 02/29/2024
BIOHORIZONS INC. BIOHORIZONS INC. 02/29/2024
ANTHOGYR AESTH. TIT. ABUT. Ø5.0 00° H2 02/09/2024
UNKNOWN ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS 08/12/2023
INSTITUT STRAUMANN AG RN SYNOCTA® CEMENT-RET. ABUTMENTS, H 5.5 06/05/2023
-
-