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
 

 
 < 
 1 
 2 
 
 
16 records meeting your search criteria returned- Product Code: KGS Product Problem: Adverse Event Without Identified Device or Use Problem

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. UNKNOWN SUSPENSORY FIXATION DEVICE 01/11/2023
SMITH & NEPHEW, INC. UNKNOWN SUSPENSORY FIXATION DEVICE 01/11/2023
SMITH & NEPHEW, INC. UNKNOWN SUSPENSORY FIXATION DEVICE 01/11/2023
SMITH & NEPHEW, INC. XTENDOBUTTON ROUND MD17 DIA 7.5 PEG 04/05/2021
SMITH & NEPHEW, INC. XTENDOBUTTON ROUND MD17 DIA 7.5 PEG 09/23/2020
SMITH & NEPHEW, INC. XTENDOBUTTON ROUND MD17 DIA 7.5 PEG 05/28/2020
-
-