• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
166 records meeting your search criteria returned- Product Code: PHX Patient Problem: Bone Fracture(s) Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DEPUY ORTHOPAEDICS INC US GLOBAL UNITE STD STEM SZ 10 09/13/2022
ZIMMER BIOMET, INC. UNKNOWN BASEPLATE 09/12/2022
ENCORE MEDICAL L.P. RSP 09/08/2022
ENCORE MEDICAL L.P. RSP 09/06/2022
ENCORE MEDICAL L.P. RSP 08/30/2022
ENCORE MEDICAL L.P. RSP 08/19/2022
ARTHREX, INC. 5.5X20MM PERIPHERAL SCREW, LOCKING 08/18/2022
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM GLENOID POLYAXIA 08/11/2022
DEPUY IRELAND - 9616671 UNK SHOULDER HUMERAL CUP DELTA XTEND 08/05/2022
MEDACTA INTERNATIONAL SA REVERSE SHOULDER SYSTEM 04.01.0152 GLENO 07/01/2022
-
-