• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
214 records meeting your search criteria returned- Product Code: HRY Product Problem: Loose or Intermittent Connection Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMET UK LTD. OXFORD CEMENTED TIBIAL TRAYS 09/14/2018
MICROPORT ORTHOPEDICS INC. EVOLUTION® MP CS INSERT 08/24/2018
MICROPORT ORTHOPEDICS INC. ADVANCE(R) II COCR TIBIAL BASE 08/23/2018
BIOMET UK LTD. UNKNOWN OXFORD TIBIAL COMPONENT 08/15/2018
MICROPORT ORTHOPEDICS INC. ADVANCE(R) II TIBIAL BASE TI NONPOROUS 07/31/2018
MICROPORT ORTHOPEDICS INC. EVOLUTION® MP TIBIAL BASE 06/25/2018
MICROPORT ORTHOPEDICS INC. EVOLUTION® MP FEMORAL COMPONENT 06/25/2018
DEPUY ORTHOPAEDICS, INC. 1818910 SIGMA HP UNI FEMORAL SZ6 LM/RL 06/19/2018
MICROPORT ORTHOPEDICS INC. ADVANCE(R) II TIBIAL BASE TI NONPOROUS 06/15/2018
AESCULAP IMPLANT SYSTEMS AS UNIVATION XF TIBIA CEMENTED T4 LM 05/30/2018
-
-