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 
 3 
 > 
 
24 records meeting your search criteria returned- Product Code: GEI Patient Problem: Wound Dehiscence Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARTHROCARE CORPORATION UNKN ENT REFLEX ULTRA PLASMA WAND AND TU 03/06/2023
ARTHROCARE CORPORATION UNKN COBLATION ENT DEV 03/06/2023
AOMORI OLYMPUS CO., LTD.OLYMPUS CO., LTD THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED 10/06/2022
ARTHROCARE CORP. UNKNOWN COBLATION ENT DEV 08/22/2022
ARTHROCARE CORP. UNKNOWN COBLATION ENT DEV 08/22/2022
ARTHROCARE CORP. UNKN COBLATION ENT DEV 08/22/2022
ETHICON ENDO-SURGERY, LLC. UNK_ENSEAL X1 TISSUE SEALER LARGE JAW 08/17/2022
ETHICON ENDO-SURGERY, LLC. UNK_ENSEAL X1 TISSUE SEALER LARGE JAW 08/09/2022
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 LARGE JAW TISSUE SEALER 08/08/2022
ETHICON ENDO-SURGERY, LLC. ENSEAL X1 LARGE JAW TISSUE SEALER 07/26/2022
-
-