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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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216 records meeting your search criteria returned- Product Code: LTI Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
APOLLO ENDOSURGERY, INC. ORBERA 365 INTRAGASTRIC BALLOON 03/19/2021
APOLLO ENDOSURGERY, INC. ORBERA365 INTRAGASTRIC BALLOON SYSTEM 03/11/2021
APOLLO ENDOSURGERY ORBERA365 INTRAGASTRIC BALLOON SYSTEM 03/10/2021
RESHAPE LIFESCIENCES LAP BAND SYSTEM 02/28/2021
ETHICON ENDO-SURGERY, INC. REALIZE BAND 02/23/2021
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON SYSTEM 01/28/2021
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON SYSTEM 01/20/2021
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON SYSTEM 01/11/2021
APOLLO ENDOSURGERY ORBERA365 INTRAGASTRIC BALLOON SYSTEM 01/08/2021
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON SYSTEM 12/15/2020
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