• 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
 

 
 < 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
386 records meeting your search criteria returned- Product Code: PHX Patient Problem: Joint Laxity Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENCORE MEDICAL L.P GLENOID, HEAD W/RETAINING SCREW, RSP, 32 12/28/2023
FX SOLUTIONS HUMELOCK REVERSED 12/26/2023
FX SOLUTIONS HUMELOCK REVERSED 12/21/2023
ENCORE MEDICAL L.P RSP MONOBLOCK SOCKET INSERT, 40MM +4MM, 12/20/2023
ZIMMER BIOMET, INC. +2MM LATERAL OFFSET 30MM POST LENGTH BAS 12/19/2023
ZIMMER BIOMET, INC. 36MM ÿ GLENOSPHERE 12/19/2023
FX SOLUTIONS EASYTECH 12/15/2023
ENCORE MEDICAL L.P GLENOID, HEAD W/RETAINING SCREW, RSP, 32 12/14/2023
FX SOLUTIONS HUMELOCK REVERSED 12/11/2023
ENCORE MEDICAL L.P. RSP 11/30/2023
-
-