• 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 
 > 
 
132 records meeting your search criteria returned- Product Code: PHX Patient Problem: Loss of Range of Motion Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN GLENOID 03/27/2024
ZIMMER BIOMET, INC. UNKNOWN HUMERAL HEAD 03/27/2024
TORNIER INC TORNIER PERFORM REVERSED LATERALIZED BAS 03/23/2024
TORNIER INC TORNIER PERFORM REVERSED LATERALIZED GLE 03/22/2024
ZIMMER BIOMET, INC. COMPREHENSIVE REVERSE SHOULDER GLENOSPHE 03/10/2024
FX SHOULDER SOLUTIONS DALLAS HUMERIS REVERSED 02/05/2024
TORNIER INC TORNIER PERFORM REVERSED LATERALIZED GLE 01/30/2024
TORNIER S.A.S. TORNIER PERFORM REVERSED LATERALIZED BAS 01/30/2024
TORNIER INC PERFORM REV INSERT SZ 3/4 39MM DIA +0 01/30/2024
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM 04.01.0172 GLENO 12/06/2023
-
-