Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
MICROPORT ORTHOPEDICS INC. ADVANCE(R) POSTERIOR STABILIZED TIBIAL I 11/21/2018
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE 11/21/2018
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE 11/21/2018
MICROPORT ORTHOPEDICS INC. ADVANCE® II COCR TIBIAL BASE 11/21/2018
MICROPORT ORTHOPEDICS INC. ADVANCE® I MEDIAL PIVOT INSERT SZ 4 LE 11/20/2018
DEPUY ORTHOPAEDICS, INC. 1818910 ENDURON NEUT 52OD X 28ID 11/20/2018
DEPUY ORTHOPAEDICS, INC. 1818910  SIGMA HP TROCHLEA SZ1 RT 11/19/2018
DEPUY ORTHOPAEDICS INC US 1818910 ACS POLY 20D 28 GR2 11/19/2018
BIOMET UK LTD. OXF ANAT BRG RT MD SIZE 5 PMA 11/15/2018
BIOMET UK LTD. OXF ANAT BRG RT LG SIZE 3 PMA 11/15/2018
-
-