• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
209 records meeting your search criteria returned- Product Code: GEI Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ERBE ELEKTROMEDIZIN GMBH ERBE ICC 200 EA 05/11/2022
ARTHROCARE CORP. EVAC 70 XTRA COBLATOR II 04/20/2022
COVIDIEN MEDICAL PRODUCTS FORCE FX 04/15/2022
ARTHROCARE CORP. UNKNOWN COBLATION ENT DEV 04/04/2022
COVIDIEN MFG DC BOULDER UNKNOWN BIZACT 03/26/2022
APYX MEDICAL CORPORATION J-PLASTY 03/25/2022
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 03/23/2022
APYX MEDICAL CORPORATION JPLASMA RENUVION 03/22/2022
COVIDIEN MEDICAL PRODUCTS FORCE FX 03/03/2022
COVIDIEN MFG DC BOULDER UNKNOWN LIGASURE INSTRUMENT 03/03/2022
-
-