• 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 
 > 
 
44 records meeting your search criteria returned- Product Code: OTO Patient Problem: Scar Tissue Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. GYNECARE GYNEMSH PS 4INX6IN 04/03/2024
COLOPLAST A/S RESTORELLE POLYPROPYLENE MESH FOR SACROC 03/27/2024
BOSTON SCIENTIFIC CORPORATION UPSYLON 11/03/2023
BOSTON SCIENTIFIC CORPORATION UPSYLON 11/01/2023
COLOPLAST A/S RESTORELLE POLYPROPYLENE MESH FOR SACROC 10/26/2023
COLOPLAST A/S RESTORELLE POLYPROPYLENE MESH FOR SACROC 07/20/2023
BOSTON SCIENTIFIC CORPORATION UPSYLON 07/18/2023
BOSTON SCIENTIFIC CORPORATION POLYFORM 06/13/2023
BOSTON SCIENTIFIC CORPORATION POLYFORM 06/12/2023
C.R. BARD, INC. (COVINGTON) -1018233 ALYTE Y-MESH GRAFT 04/17/2023
-
-