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

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESHAPE LIFESCIENCES LAP-BAND SYSTEM 05/24/2023
RESHAPE LIFESCIENCES LAP-BAND SYSTEM 06/13/2022
RESHAPE LIFESCIENCES LAP-BAND SYSTEM 06/13/2022
APOLLO ENDOSURGERY, INC. ORBERA® INTRAGASTRIC BALLOON SYSTEM 12/21/2021
APOLLO ENDOSURGERY, INC. ORBERA® INTRAGASTRIC BALLOON SYSTEM 02/24/2020
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 09/24/2019
APOLLO ENDOSURGERY, INC. LAP-BAND SYSTEM 10/10/2018
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 07/25/2018
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 07/24/2018
APOLLO ENDOSURGERY, INC LAP-BAND SYSTEM 07/18/2018
-
-