• 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 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
448 records meeting your search criteria returned- Product Code: MJO Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 09/04/2020
LDR MÉDICAL IMPLANT MOBIC M ST 15X15 H5 US 08/25/2020
AESCULAP AG ACTIV L INF.PLATE SIZE L 0/SPIKES 08/11/2020
AESCULAP AG ACTIV L SUP.PLATE SIZE L 11/SPIKES 08/11/2020
AESCULAP AG ACTIV L SUP.PLATE SIZE M 6/SPIKES 07/07/2020
AESCULAP AG ACTIV L PE-INLAY 8.5MM 07/07/2020
AESCULAP AG ACTIV L SUP.PLATE SIZE M 6/SPIKES 07/07/2020
AESCULAP AG COLLECT.NO.QAS SPINE ANTERIOR STABILIS. 06/26/2020
AESCULAP AG ACTIV L SUP.PLATE SIZE S 6/SPIKES 05/21/2020
AESCULAP AG ACTIV L INF.PLATE S1 SIZE S 5/SPIKES 05/21/2020
-
-