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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
167 records meeting your search criteria returned- Product Code: KMW Product Problem: Overheating of Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NAKANISHI INC. NSK 09/23/2020
GYRUS ACMI, INC MULTIDEBRIDER HANDPIECE, STRAIGHT 08/25/2020
NAKANISHI INC. NSK 03/25/2020
NAKANISHI INC. NSK 03/25/2020
NAKANISHI INC. NSK 03/23/2020
NAKANISHI INC. NSK 03/23/2020
NAKANISHI INC. NSK 12/06/2019
NAKANISHI INC. NSK 12/02/2019
NAKANISHI INC. NSK 12/02/2019
NAKANISHI INC. NSK 11/25/2019
-
-