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 
 9 
 10 
 > 
 
136 records meeting your search criteria returned- Product Code: KXA Patient Problem: Reaction Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. CONSERVE(R) SF W/HM TECH. FEMORAL COMPON 04/30/2018
ZIMMER BIOMET, INC. UNKNOWN RECAP FEMORAL HEAD 04/15/2018
ZIMMER BIOMET, INC. RECAP CEMENT FMRL HD RESUR46MM 04/15/2018
ZIMMER BIOMET, INC. RECAP CEMENT FMRL HD RESUR44MM 04/13/2018
ZIMMER BIOMET, INC. UNKNOWN STEM 04/10/2018
ZIMMER BIOMET, INC. RECAP CEMENT FMRL HD RESUR52MM 03/26/2018
MICROPORT ORTHOPEDICS INC. CONSERVE® CUP 03/14/2018
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN LFIT ANATOMIC COCR V40 FEMORAL H 02/20/2018
STRYKER ORTHOPAEDICS-MAHWAH MERIDIAN FEMORAL STEM 01/29/2018
MICROPORT ORTHOPEDICS INC. CONSERVE® TOTAL NECK SLEEVE 01/29/2018
-
-