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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
409 records meeting your search criteria returned- Product Code: NBH Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US ARTHRO PUSHER/CUTTER *EA 01/17/2020
DEPUY MITEK LLC US ARTHRO GRASPER PEN 35 UP *EA 01/14/2020
DEPUY MITEK LLC US ARTHRO GRASPER PEN STR *EA 01/14/2020
DEPUY MITEK LLC US ARTHRO PUSHER/CUTTER *EA 01/06/2020
DEPUY MITEK LLC US ARTHRO PUSHER/CUTTER *EA 01/03/2020
MEDOS INTERNATIONAL SàRL ARTHRO PUSHER/CUTTER *EA 01/03/2020
DEPUY MITEK LLC US ARTHRO GRASPER PEN 35 UP *EA 01/03/2020
DEPUY MITEK LLC US ARTHRO SIXTER-LEFT *EA 01/03/2020
DEPUY MITEK LLC US TUNNEL DILATOR 6.0MM *EA 01/02/2020
DEPUY MITEK LLC US TUNNEL DILATOR 8.0MM *EA 12/30/2019
-
-