• 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 
 7 
 8 
 9 
 10 
 > 
 
500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN DURACON TIBIAL BASEPLATE 08/27/2024
MICROPORT ORTHOPEDICS INC. EVOLUTION® REV TIB MOD KEEL 06/28/2024
MICROPORT ORTHOPEDICS INC. EVOLUTION® CANAL FILL STEM EXT15MM X 10 06/28/2024
EXACTECH, INC. OPTETRAK LOGIC 06/27/2024
Unknown Manufacturer EVOLUTION® REV TIB BASE NONPORSIZE 6 ST 06/27/2024
EXACTECH, INC. LOGIC FEMORAL 06/26/2024
STRYKER ORTHOPAEDICS-MAHWAH SERIES 7000 STANDARD TIBIA 06/13/2024
STRYKER ORTHOPAEDICS-MAHWAH TRITANIUM BPLATE TRIATHLON S3 06/13/2024
SMITH & NEPHEW, INC. UNKN GENESIS II TOTAL KNEE PAT COMP 04/25/2024
MICROPORT ORTHOPEDICS INC. ADVANCE® II MEDIAL PIVOT TIBIAL INSERT S 04/19/2024
-
-