• 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
ZIMMER MANUFACTURING B.V. NEXGEN ALL POLY PETELLA STANDARD CEMENTE 04/24/2024
SMITH & NEPHEW, INC. UNKN ORTHOPAEDIC RECONSTRUCTION DEV 03/04/2024
ZIMMER BIOMET, INC. PERSONA REVISION VIVACIT-E CCK ARTICULAR 02/12/2024
SMITH & NEPHEW, INC. GII CR DEEP FLEX ISRT S5-6 9M 01/31/2024
ZIMMER BIOMET, INC. VNGD SSK PSC FMRL STEM SCREW 01/29/2024
DEPUY ORTHOPAEDICS INC US UNIVERSAL STEM 115X18MM FLUTED 01/19/2024
ZIMMER MANUFACTURING B.V. ALL POLY PATELLA STANDARD CEMENTED SIZE 12/29/2023
DEPUY IRELAND - 9616671 UNK ATTUNE FEMORAL 12/19/2023
DEPUY IRELAND - 9616671 UNK ATTUNE KNEE TIBIAL INSERT 12/19/2023
DEPUY IRELAND - 9616671 ATTUNE PS FB INSRT SZ 8 8MM 12/12/2023
-
-