• 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
131 records meeting your search criteria returned- Product Code: PHX Patient Problem: Implant Pain Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TORNIER INC UNKNOWN TORNIER HRS ASSEMBLY SCREW 11/14/2023
TORNIER INC TORNIER HRS LOCKING CAP 11/14/2023
TORNIER INC - MHRA ORG ID:33836 TORNIER PERFORM REVERSED STANDARD GLENOS 11/07/2023
TORNIER INC TORNIER PERFORM REVERSED LATERALIZED BAS 11/07/2023
FX SHOULDER SOLUTIONS DALLAS FXV135 REVERSE 11/03/2023
ENCORE MEDICAL L.P ALTIVATE REVERSE, HUMERAL STEM, STANDARD 10/31/2023
FX SOLUTIONS REVERSED SHOULDER PROTHESIS 10/30/2023
ENCORE MEDICAL L.P GLENOID, HEAD W/RETAINING SCREW, RSP, 36 10/14/2023
TORNIER S.A.S. UNKNOWN LOCKING SCREW 10/10/2023
TORNIER S.A.S. AEQUALIS REVERSED CEMENTLESS METAPHYSIS 10/10/2023
-
-