• 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
 

 
 
8 records meeting your search criteria returned- Product Code: FTL Product Problem: Device Appears to Trigger Rejection Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COLOPLAST A/S RESTORELLE DIRECTFIX 07/17/2020
W.L. GORE & ASSOCIATES GORE DUALMESH BIOMATERIAL 05/22/2020
W.L. GORE & ASSOCIATES GORE-TEX® SOFT TISSUE PATCH 05/20/2020
SOFRADIM PRODUCTION SAS MESH SOFRADIM - UGYTEX¿ 08/01/2018
W.L. GORE & ASSOCIATES GORE® DUALMESH® PLUS BIOMATERIAL WITH HO 06/27/2018
W.L. GORE & ASSOCIATES GORE DUALMESH PLUS BIOMATERIAL 06/27/2018
W.L. GORE & ASSOCIATES GORE DUALMESH BIOMATERIAL 06/27/2018
ETHICON INC. PROCEED*SURG MESH/MULTI LYR 03/07/2018
-
-