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 
 > 
 
31 records meeting your search criteria returned- Product Code: KXA Product Problem: Insufficient Information Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MICROPORT ORTHOPEDICS INC. CONSERVE TOTAL SHORT NECK SLEEVE ADDED C 03/18/2020
ZIMMER GMBH DUROM 03/10/2020
ZIMMER GMBH RESURFACING DUROM METASUL HEAD 03/06/2020
BIOMET UK LTD. DELTA CER FEM HD 32/-3MM T1 02/20/2020
MICROPORT ORTHOPEDICS INC. CONSERVE TOTAL SHORT NECK SLEEVE ADDED C 02/17/2020
MICROPORT ORTHOPEDICS INC. CONSERVE® CEMENTLESS FEMORAL COMPONENT 4 02/03/2020
BIOMET UK LTD. UNK RECAP MAGNUM 12/05/2019
ZIMMER GMBH ALLOCLASSIC SL STEM HIP 10/31/2019
ZIMMER BIOMET, INC. UNKNOWN ZIMMER TAPER STEM 10/25/2019
MICROPORT ORTHOPEDICS INC. CONSERVE® FEMORAL RESURFACING HEAD 46MM 09/11/2019
-
-