• 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 
 > 
 
58 records meeting your search criteria returned- Product Code: MEH Product Problem: Fracture Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDACTA INTERNATIONAL SA LINER: VERSAFITCUP DM DOUBLE MOBILITY HC 11/19/2021
STRYKER ORTHOPAEDICS-MAHWAH RESTORATION ADM X3 INS 28/48 11/07/2021
STRYKER ORTHOPAEDICS-MAHWAH RESTORATION ADM X3 INS 28/48 10/20/2021
CORIN MEDICAL TRIFIT CF 10/04/2021
CORIN MEDICAL TRINITY 09/06/2021
STRYKER ORTHOPAEDICS-MAHWAH ABGII. MODULAR STEM 07/22/2021
STRYKER ORTHOPAEDICS-MAHWAH UNKNOWN ABGII FEMORAL NECK 07/22/2021
STRYKER ORTHOPAEDICS-MAHWAH ABGII MODULAR LONG NECK 06/25/2021
STRYKER ORTHOPAEDICS-MAHWAH ABGII. MODULAR STEM 06/25/2021
ZIMMER BIOMET, INC. SYSTEM RASP LONG POST SIZE 4 06/25/2021
-
-