• 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 
 > 
 
13 records meeting your search criteria returned- Product Code: NHA Product Problem: Use of Device Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS MULTI-UNIT ABUTMENT SCREW 10/31/2022
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS ABUTMENT SCREW 10/31/2022
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS MULTI-UNIT ABUTMENT 10/31/2022
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS ABUTMENT 07/29/2022
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS IMPLANT SYSTEM ABUTMENTS 05/05/2022
INTRA-LOCK IMPLANT SYSTEMS INTRA-LOCK IMPLANT SYSTEMS IMPLANT PROST 05/05/2022
INTRA-LOCK IMPLANT SYSTEMS INTRA-LOCK IMPLANT SYSTEMS IMPLANT PROST 05/05/2022
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS IMPLANT SYSTEMS 07/30/2021
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS IMPLANT SYSTEMS 07/30/2021
BIOHORIZONS IMPLANT SYSTEMS BIOHORIZONS HEX ABUTMENTS 04/30/2021
-
-