• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
5 records meeting your search criteria returned- Product Code: KXE Report Date From: 1/1/2017 Report Date To: 12/31/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. UNKNOWN SMOOTH PEG 11/02/2017
ZIMMER BIOMET, INC. UNKNOWN ULNAR STEM 11/02/2017
ZIMMER BIOMET, INC. UNKNOWN NEXEL PROXIMAL ULNA 10/26/2017
ZIMMER BIOMET, INC. UNKNOWN ULNAR STEM 09/21/2017
ZIMMER, INC. UNKNOWN ULNAR 09/06/2017
-
-