• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 > 
 
75 records meeting your search criteria returned- Product Code: EFB Product Problem: Detachment Of Device Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DENTSPLY PROFESSIONAL MIDWEST TRADITION PB NON FIBER OPTIC 02/10/2016
DENTSPLY PROFESSIONAL MIDWEST TRADITION PB NON FIBER OPTIC 10/23/2015
NAKANISHI INC. MASTER II MINI PUSH BUTTON 09/08/2015
NAKANISHI INC. N5000 09/08/2015
DENTSPLY PROFESSIONAL MIDWEST TRADITION FIBER OPTIC 09/03/2015
NAKANISHI, INC. (NSK) NSK SX-SU03 07/02/2015
NAKANISHI INC. (NSK) NSK TI-MAX A600LC 05/26/2015
NAKANISHI INC. (NSK) TI-SU03 GC 05/26/2015
NAKANISHI INC. (NSK) NSK X-SL 05/26/2015
NAKANISHI, INC. NSK TI-MAX AK450L SU 05/08/2015
-
-