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

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
 

 
 
6 records meeting your search criteria returned- Product Code: OTO Patient Problem: Perforation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COLOPLAST A/S RESTORELLE  Y 09/14/2022
COLOPLAST A/S RESTORELLE L 12/12/2020
COLOPLAST A/S RESTORELLE Y 12/08/2020
ETHICON INC. GYNECARE UNKNOWN PRODUCT 11/30/2020
BOSTON SCIENTIFIC CORPORATION POLYFORM 04/22/2019
BOSTON SCIENTIFIC CORPORATION POLYFORM 04/21/2019
-
-