• 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
 

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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN COMPREHENSIVE REVERSE HUMERAL ST 01/28/2021
ZIMMER BIOMET, INC. UNK COMPREHENSIVE REVERSE GLENOSPHERE 01/28/2021
TORNIER INC AEQUALIS PERFORM REVERSE SHOULDER SYSTEM 08/25/2020
TORNIER INC AEQUALIS PERFORM REVERSE SHOULDER SYSTEM 06/19/2020
TORNIER INC AEQUALIS PERFORM REVERSE SHOULDER SYSTEM 05/29/2019
ENCORE MEDICAL L.P. RSP SHOULDER 02/15/2019
-
-