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 
 3 
 4 
 5 
 6 
 > 
 
58 records meeting your search criteria returned- Product Code: FTL Product Problem: Microbial Contamination of Device Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
W. L. GORE & ASSOCIATES, INC. GORE-TEX® SOFT TISSUE PATCH 10/26/2022
W. L. GORE & ASSOCIATES, INC. GORE® DUALMESH® BIOMATERIAL 04/22/2022
W.L. GORE & ASSOCIATES GORE MYCROMESH BIOMATERIAL 09/14/2021
W. L. GORE & ASSOCIATES, INC. GORE BIO-A TISSUE REINFORCEMENT 07/27/2021
ATRIUM MEDICAL CORPORATION C-QUR EDGE 02/04/2021
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 01/28/2021
ATRIUM MEDICAL CORPORATION C-QUR MESH 09/21/2020
ATRIUM MEDICAL CORPORATION C-QUR CENTRIFX 08/05/2020
W.L. GORE & ASSOCIATES GORE SYNECOR INTRAPERITONEAL BIOMATERIAL 06/24/2020
W.L. GORE & ASSOCIATES GORE SYNECOR INTRAPERITONEAL BIOMATERIAL 05/15/2020
-
-