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 
 > 
 
28 records meeting your search criteria returned- Product Code: GCJ Product Problem: Device Difficult to Setup or Prepare Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
US SURGICAL PUERTO RICO MULTIFIRE ENDO HERNIA 03/13/2023
US SURGICAL PUERTO RICO MULTIFIRE ENDO HERNIA 03/06/2023
DAVIS & GECK CARIBE LTD VERSAONE 01/25/2023
COVIDIEN LP LLC NORTH HAVEN LAPRO-CLIP 07/27/2022
COVIDIEN LP LLC NORTH HAVEN LAPRO-CLIP 05/11/2022
US SURGICAL PUERTO RICO ENDO UNIVERSAL 65 04/12/2022
US SURGICAL PUERTO RICO SPACEMAKER 01/26/2022
DAVIS & GECK CARIBE LTD VERSAONE 01/11/2022
US SURGICAL PUERTO RICO PROTACK 12/23/2021
COVIDIEN LP LLC NORTH HAVEN LAPRO-CLIP 07/08/2021
-
-