• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
96 records meeting your search criteria returned- Product Code: KWS Product Problem: Inadequacy of Device Shape and/or Size Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL, L.P. RSP SHOULDER 06/04/2015
TORNIER SAS AEQUALIS REVERSED FRACTURE HUMERAL INSER 05/06/2015
TORNIER SAS AEQUALIS REVERSED FRACTURE HUMERAL STEM 05/06/2015
TORNIER SAS AEQUALIS REVERSED II CENTERED GLENOID SP 05/06/2015
ENCORE MEDICAL, L.P. TURON SHOULDER 05/05/2015
TORNIER SAS AEQUALIS REVERSED 03/24/2015
DEPUY ORTHOPAEDICS, INC. 1818910 UNKNOWN DEPUY UNITE 48X21 ECCENRIC HEAD 03/02/2015
ZIMMER GMBH AS HUMERAL STEM FX 10-130 01/30/2015
BIOMET ORTHOPEDICS UNKNOWN BIO-MODULAR HEAD 01/16/2015
BIOMET ORTHOPEDICS BIO-MOD 44X17MM HD 4MM OFFSET 12/15/2014
-
-