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

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 
 
 
11 records meeting your search criteria returned- Product Code: LTI Patient Problem: Ulceration Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
Unknown Manufacturer INTRA-GASTRIC BALLOON 08/24/2018
RESHAPE MEDICAL INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 02/02/2018
RESHAPE MEDICAL INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 11/10/2017
RESHAPE MEDICAL INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 09/15/2017
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 09/15/2017
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON 11/18/2016
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON 07/16/2016
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON 05/12/2016
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON 04/08/2016
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON 04/01/2016
-
-