• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: KWA Patient Problem: Unequal Limb Length Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZIMMER BIOMET, INC. ECHO POR FMRL RED NC 12X140MM 04/01/2024
ZIMMER BIOMET, INC. M2A MAGNUM 42-50M TPR INSRT +6 04/01/2024
ZIMMER BIOMET, INC. M2A-MAGNUM MOD HD SZ 50MM 04/01/2024
ZIMMER BIOMET, INC. M2A-MAGNUM 12/14 TPR 42-50 -3 12/06/2023
ZIMMER BIOMET, INC. ARCOS CON SZ A STD 80MM 09/07/2023
ZIMMER BIOMET, INC. ARCOS 15X190MM SPL TPR DIST 09/07/2023
ZIMMER SWITZERLAND MANUFACTURING GMBH UNKNOWN METASUL HEAD 06/26/2023
ZIMMER BIOMET, INC. M2A 38MM MOD HD STD NK 10/06/2022
ZIMMER BIOMET, INC. M2A 1 PC SHELL 38MMX50MM 10/06/2022
ZIMMER BIOMET, INC. UNKNOWN STEM 06/28/2022
-
-