• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
348 records meeting your search criteria returned- Product Code: GEH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ENTELLUS MEDICAL, INC. CLARIFIX 05/19/2023
UNITED STATES ENDOSCOPY GROUP, INC. TRUFREEZE SPRAY CRYOTHERAPY SYSTEM 04/13/2023
BTG ROUND LAKE ICEFX CRYOABLATION SYSTEM US 04/11/2023
ATRICURE, INC. CRYOFORM CRYOICE CRYOABLATION PROBE 04/07/2023
ENTELLUS MEDICAL, INC. CLARIFIX 03/20/2023
ENTELLUS MEDICAL, INC. CLARIFIX 03/14/2023
BTG YOKNEAM ICEPEARL 2.1 CX 90 DEGREE NEEDLE 03/01/2023
BTG YOKNEAM ICEPEARL 2.1 CX 90 DEGREE NEEDLE 02/20/2023
BTG YOKNEAM ICEROD CX 90 DEGREE NEEDLE/VL 02/17/2023
ENTELLUS MEDICAL, INC. UNKNOWN_INSTRUMENTS_PRODUCT 12/19/2022
-
-