Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
77 records meeting your search criteria returned- Product Code: PHX Product Problem: Naturally Worn Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHREX, INC. 5.5X16MM PERIPHERAL SCREW, LOCKING 06/02/2022
ARTHREX, INC. 33/24 GLENOSPHERE 06/02/2022
ARTHREX, INC. 25MM CENTRAL SCREW, MODULAR 06/02/2022
ARTHREX, INC. 20MM CENTRAL SCREW, MODULAR 06/02/2022
ARTHREX, INC. 24MM BASEPLATE, MODULAR 06/02/2022
ARTHREX, INC. 24MM BASEPLATE, MODULAR 06/02/2022
ARTHREX, INC. 36 +3 / 33 COMBO HUMERAL INSERT 06/02/2022
ARTHREX, INC. 25MM CENTRAL SCREW, MODULAR 05/23/2022
ARTHREX, INC. 5.5X16MM PERIPHERAL SCREW, LOCKING 05/23/2022
ARTHREX, INC. 5.5X24MM PERIPHERAL SCREW, LOCKING 05/23/2022
-
-