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

MAUDE - Manufacturer and User Facility Device Experience
  • 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: FTL Product Problem: Failure to Osseointegrate Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 10/21/2021
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 10/21/2021
ATRIUM MEDICAL CORPORATION MESH PROLITE SHEETS 10/18/2021
ATRIUM MEDICAL CORPORATION C-QUR TACSHIELD 01/18/2021
ATRIUM MEDICAL CORPORATION C-QUR MESH 01/05/2021
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 11/24/2020
ATRIUM MEDICAL CORPORATION C-QUR CENTRI FX 10/12/2020
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 10/12/2020
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 09/21/2020
ATRIUM MEDICAL CORPORATION C-QUR MOSAIC 09/07/2020
-
-