• 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: LTI Patient Problem: Dizziness Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
APOLLO ENDOSURGERY COSTA RICA S.R.L. ORBERA ENDOSCOPY / ORBERA 02/28/2022
APOLLO ENDOSURGERY COSTA RICA S.R.L. ORBERA 12/27/2021
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 08/20/2019
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 04/10/2019
APOLLO ENDOSURGERY, INC ORBERA INTRAGASTRIC BALLOON SYSTEM 04/02/2018
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON 02/20/2018
RESHAPE RESHAPE BALLOON SYSTEM (INTEGRATED DUAL) 08/11/2017
ALLERGAN (COSTA RICA) ORBERA INTRAGASTRIC BALLOON 11/06/2015
ALLERGAN LAP-BAND ADJUSTABLE GASTRIC BANDING SYST 07/16/2015
ALLERGAN LAP-BAND AP ADJUSTABLE GASTRIC BANDING S 07/10/2015
-
-