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
 

 
 
9 records meeting your search criteria returned- Product Code: KDC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
N.V. ORGANON NEXPLANON IMPLANTED ROD (DEVICE) 02/08/2023
ETHICON INC. MERS TAPE WHT 12INX3/16IN D/A CTX 02/03/2022
ETHICON INC. MERS TAPE WHT 12INX3/16IN D/A CTX 01/26/2022
ETHICON INC. NYLON TAPE UNKNOWN PRODUCT 10/09/2021
ETHICON INC. MERS TAPE WHT 12INX3/16IN D/A CTX 09/22/2021
ETHICON INC. MERS TAPE WHT 12INX3/16IN D/A CTX 09/21/2021
ETHICON INC. MERSILENE TAPE UNKNOWN PRODUCT 03/05/2019
ETHICON INC. MERSILENE TAPE UNKNOWN PRODUCT 01/22/2019
ETHICON INC. MERSILENE TAPE UNKNOWN PRODUCT 01/08/2019
-
-