• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
13 records meeting your search criteria returned- Product Code: NTE Patient Problem: Injury Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN SPIDER FX 10/28/2020
COVIDIEN SPIDER FX 10/15/2020
COVIDIEN SPIDER FX 10/09/2020
COVIDIEN SPIDER FX 09/21/2020
INVATEC SPA MO.MA 07/09/2020
INVATEC SPA SPIDER FX 07/09/2020
COVIDIEN SPIDER FX 01/31/2020
COVIDIEN SPIDER FX 12/10/2019
COVIDIEN SPIDER FX 12/10/2019
COVIDIEN SPIDER FX 12/02/2019
-
-