• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
7 records meeting your search criteria returned- Product Code: DRX Patient Problem: Localized Skin Lesion Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONMED CORPORATION SOFTRACE 03/07/2024
CARDINAL HEALTH KENDALL 02/12/2024
LEONHARD LANG GMBH PHILIP 06/07/2023
NEOTECH PRODUCTS LLC NEOLEAD MICRO 04/26/2023
LEONHARD LANG GMBH ASMUTH 07/19/2022
CARDINAL HEALTH 1050NPSM KCAT 3/PK 100 PK/CASE 10/20/2021
LEONHARD LANG GMBH SKINTACT 09/30/2020
-
-