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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: LTI Patient Problem: Pulmonary Embolism Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
RESHAPE LIFESCIENCES LAP-BAND SYSTEM 01/17/2023
APOLLO ENDOSURGERY, INC. ORBERA365 INTRAGASTRIC BALLOON SYSTEM 06/12/2019
APOLLO ENDOSURGERY, INC. ORBERA365 INTRAGASTRIC BALLOON SYSTEM 06/12/2019
APOLLO ENDOSURGERY, INC. LAP-BAND SYSTEM 11/20/2018
APOLLO ENDOSURGERY, INC ORBERA INTRAGASTRIC BALLOON SYSTEM 04/02/2018
APOLLO ENDOSURGERY ORBERA INTRAGASTRIC BALLOON 02/20/2018
RESHAPE MEDICAL INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 10/20/2017
APOLLO ENDOSURGERY, INC. ORBERA INTRAGASTRIC BALLOON SYSTEM 03/09/2017
APOLLO ENDOSURGERY LAP BAND SYSTEM 01/27/2017
RESHAPE MEDICAL, INC. RESHAPE INTEGRATED DUAL BALLOON SYSTEM 01/24/2017
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