• 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: GEI Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INMODE LTD. IN MODE MORPHEUS 8 05/24/2023
APYX MEDICAL CORPORATION RENUVION 05/10/2023
INMODE LTD. MORPHEUS8 05/02/2023
ETHICON ENDO-SURGERY, LLC. ENSEAL 45 CM SHAFT, CURVED JAW 03/30/2023
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 CURVED 37CM SHAFT 03/15/2023
3M HEALTH CARE 3M¿ UNIVERSAL ELECTROSURGICAL PADS 03/15/2023
STRYKER ENDOSCOPY-SAN JOSE RF 2 PROBES, 90-S 02/23/2023
MEGADYNE MEDICAL PRODUCTS, INC. MEGASOFT UNIVERSAL PLUS 01/18/2023
MEGADYNE MEDICAL PRODUCTS, INC. MEGASOFT UNIVERSAL PLUS 01/13/2023
MEGADYNE MEDICAL PRODUCTS, INC. MEGASOFT UNIVERSAL PLUS 01/06/2023
-
-