• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 
 
60 records meeting your search criteria returned- Product Code: HRY 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
DEPUY ORTHOPAEDICS, INC. SIGMA HP UNI TIB TRAY SZ3 LMRL 08/09/2016
BIOMET ORTHOPEDICS VANGUARD M UNI FEMORAL LG 06/30/2016
BIOMET ORTHOPEDICS VANGUARD M UNI FMRL MED 06/29/2016
BIOMET ORTHOPEDICS BIOMET CC I-BEAM TRAY 71MM 05/09/2016
DEPUY ORTHOPAEDICS, INC. 1818910 SIGMA HP UNI TIB TRAY SZ3 LMRL 10/02/2015
BIOMET ORTHOPEDICS REPICCI TIBIAL 37X6.5MM 04/20/2015
BIOMET UK LTD. OXF UNI TIB TRAY SZ D LM PMA 11/26/2014
1219655 DEPUY-RAYNHAM PRSVN ALLPOLY TIB RMLL S3 7MM 09/25/2014
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN_RECONSTRUCTIVE_PRODUCT 09/24/2014
1219655 DEPUY-RAYNHAM SIGMA HP UNI TIB TRAY SZ3 RMLL 08/07/2014
-
-