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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TOGO MEDIKIT CO., LTD. SUPER SHEATH 05/23/2024
MERIT MEDICAL SYSTEMS INC. PRELUDE®. SHEATH 04/23/2024
MERIT MEDICAL SYSTEMS INC. PRELUDE® 04/16/2024
MERIT MEDICAL SYSTEMS MEXICO MICRO ACE¿ ADVANCED MICRO ACCESS SYSTEM 04/10/2024
MERIT MEDICAL SYSTEMS MEXICO MERIT MAK¿ COAXIAL MINI ACCESS KIT 04/09/2024
MERIT MEDICAL SYSTEMS, INC. PRELUDE SHEATH INTRODUCER 03/26/2024
ANGIODYNAMICS, INC ANGIODYNAMICS 03/04/2024
CORDIS US CORP. AVANTI 01/04/2024
CORDIS US CORP. AVANTI TRANSRADIAL 12/26/2023
MERIT MEDICAL SYSTEMS INC. PRELUDE RADIAL SHEATH 12/12/2023
-
-