• 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
 

 
 < 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 > 
 
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 BIOMET, INC. UNKNOWN HEAD 08/20/2018
. UNKNOWN CUP 08/17/2018
ZIMMER BIOMET, INC. G7 DUAL MOBILITY LINER 08/17/2018
ZIMMER BIOMET, INC. UNKNOWN CUP 08/17/2018
ZIMMER BIOMET, INC. UNKNOWN TRILOGY LINER 08/17/2018
ZIMMER BIOMET, INC. ACTIVE ARTICULATION HEAD 08/16/2018
ZIMMER BIOMET, INC. G7 LINER 08/16/2018
ZIMMER BIOMET, INC. UNKNOWN MAGNUM CUP 08/13/2018
ZIMMER BIOMET, INC. UNKNOWN HEAD 08/13/2018
ZIMMER BIOMET, INC. UNKNOWN STEM 08/13/2018
-
-