• 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
 

 
 
5 records meeting your search criteria returned- Product Code: PHX Patient Problem: Tissue Breakdown Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN GLENOID 11/23/2021
ZIMMER BIOMET, INC. UNKNOWN HUMERAL HEAD 11/23/2021
ZIMMER BIOMET, INC. UNKNOWN GLENOID 11/19/2021
ARTHREX, INC. 42 +4 LAT/24 GLENOSPHERE 12/20/2019
ARTHREX, INC. UNIVERS REVERS APEX STEM, SIZE 7 12/20/2019
-
-