• 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 
 > 
 
214 records meeting your search criteria returned- Product Code: PHX Product Problem: Loosening of Implant Not Related to Bone-Ingrowth Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN PERIPHERAL SCREW 04/16/2024
ZIMMER BIOMET, INC. UNKNOWN GLENOID 04/16/2024
EXACTECH, INC. EQUINOXE SMALL GLENOID PLATE 04/11/2024
ZIMMER BIOMET, INC. UNK GLENOSPHERE 04/11/2024
ZIMMER BIOMET, INC. UNKNOWN COMPRESS MINI 04/01/2024
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM THREADED GLENOID 03/20/2024
ZIMMER BIOMET, INC. UNK TM REVERSE BASEPLATE 03/12/2024
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM THREADED GLENOID 03/07/2024
ARTHREX, INC. 24MM BASEPLATE, 10° FULL AUG, ST 02/08/2024
EXACTECH, INC. SMALL GLENOID PLATE 02/06/2024
-
-