• 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 
 > 
 
218 records meeting your search criteria returned- Product Code: MNH Patient Problem: Failure of Implant Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - RODS 09/25/2020
GLOBUS MEDICAL, INC. ROD 09/24/2020
MEDOS INTERNATIONAL SàRL CH SINGLE-INNER SETSCREW 09/22/2020
MEDOS INTERNATIONAL SàRL CH EXP TI UNI SCREW 6MM X 50MM 09/22/2020
GLOBUS MEDICAL, INC. CREO 09/14/2020
DEPUY SPINE INC MMSI SINGLE INNER SETSCREW 06/02/2020
OBERDORF SYNTHES PRODUKTIONS GMBH ROD 6 HARD L400 TI 05/11/2020
OBERDORF SYNTHES PRODUKTIONS GMBH ROD 6 HARD L400 TI 05/11/2020
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - MONO/POLYAXIAL SCREWS: USS 04/22/2020
OBERDORF SYNTHES PRODUKTIONS GMBH UNK - RODS: USS 04/22/2020
-
-