• 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 
 > 
 
12 records meeting your search criteria returned- Product Code: GDT Product Problem: Device Slipped Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, INC. ETHICON ENDO-SURGERY STAPLER REGULAR STA 04/18/2023
COVIDIEN LP APPOSE ULC 08/25/2020
ETHICON ENDO-SURGERY, LLC. PROXIMATE*PLUS MD SKIN STPLR 08/18/2019
ETHICON ENDO-SURGERY, LLC. PROXIMATE*SKIN STAPLER-WIDE 11/27/2018
ETHICON ENDO-SURGERY, LLC. PROXIMATE*SKIN STAPLER-WIDE 11/27/2018
ETHICON ENDO-SURGERY, LLC. PROXIMATE*SKIN STAPLER-WIDE 11/27/2018
ETHICON ENDO-SURGERY, LLC. PROXIMATE*SKIN STAPLER-WIDE 11/27/2018
ETHICON ENDO-SURGERY, LLC. PROXIMATE*SKIN STAPLER-WIDE 11/27/2018
TELEFLEX MEDICAL HEMOLOK ML CLIPS 3/CART 42/BOX 06/25/2018
ETHICON ENDO-SURGERY, INC. PROXIMATE 35 04/12/2016
-
-