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
 

 
 
5 records meeting your search criteria returned- Product Code: GDC Product Problem: Malposition of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. SPIDER 2 TENET 7615 07/28/2020
STERIS CORPORATION CMAX 07/26/2019
MIZUHO OSI JACKSON TABLE WITH FLAT TOP 12/11/2017
STERIS CORPORATION - MONTGOMERY CMAX SURGICAL TABLE 08/24/2017
SKYTRON, LLC. HERCULES 03/24/2017
-
-