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
 

 
 
7 records meeting your search criteria returned- Product Code: HBT Product Problem: Failure to Align Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CONMED UTICA REFLEX ELC,20M/L CLPS,10/11MM 02/01/2023
CONMED UTICA REFLEX ELC,20M/L CLPS,10/11MM 09/01/2021
CONMED UTICA REFLEX ELC,20M/L CLPS,10/11MM 09/01/2021
CONMED UTICA REFLEX ELC,20M/L CLPS,10/11MM 08/31/2021
CONMED CORPORATION REFLEX ELC,20M/L CLPS,10/11MM 04/01/2021
ETHICON ENDO-SURGERY, LLC. LIGACLIP*ENDO MED/LG APPLIER 06/13/2019
TELEFLEX MEDICAL HEM-O-LOK XL ENDO 10, APPLIER 08/04/2015
-
-