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

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
 

 
 
 1 
 2 
 > 
 
16 records meeting your search criteria returned- Product Code: GEI Patient Problem: Deformity/ Disfigurement Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
VIOL CO., LTD. SYLFIRM X 02/13/2024
APYX MEDICAL CORPORATION RENUVION 01/12/2024
SOLTA MEDICAL, INC THERMAGE FLX (TG-3A) SYSTEM AND ACCESSOR 12/06/2023
INMODE LTD. MORPHEUS8 08/29/2023
BENEV / VIOL CO., LTD. SYLFIRM X 06/13/2023
INMODE LTD. MORPHEUS 8 01/06/2023
APYX MEDICAL CORPORATION RENUVION 01/04/2023
INMODE LTD. MORPHEUS8 RADIOFREQUENCY MICRONEEDLING 12/20/2022
APYX MEDICAL CORPORATION J PLASMA RENUVION 11/30/2022
APYX MEDICAL CORPORATION JPLASMA RENUVION 07/26/2022
-
-