• 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 
 > 
 
65 records meeting your search criteria returned- Product Code: FTL Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. -121364 VENTRALIGHT ST W/ ECHO 03/15/2022
ATRIUM MEDICAL CORPORATION C-QUR PROLITE 02/07/2022
ATRIUM MEDICAL CORPORATION PROLITE MESH 01/13/2022
ATRIUM MEDICAL CORPORATION PROLITE MESH 01/13/2022
DAVOL INC., SUB. C.R. BARD, INC. -121364 VENTRALIGHT ST W/ ECHO 01/13/2022
W. L. GORE & ASSOCIATES, INC. GORE® BIO-A® TISSUE REINFORCEMENT 07/27/2021
ATRIUM MEDICAL CORPORATION PROLITE MESH 06/22/2020
W.L. GORE & ASSOCIATES GORE-TEX® SOFT TISSUE PATCH 05/20/2020
W.L. GORE & ASSOCIATES GORE® SYNECOR INTRAPERITONEAL BIOMATERIA 02/20/2020
W.L. GORE & ASSOCIATES GORE-TEX SOFT TISSUE PATCH 01/30/2020
-
-