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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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105 records meeting your search criteria returned- Product Code: FDI Product Problem: Entrapment of Device Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 02/26/2024
BOSTON SCIENTIFIC CORPORATION CAPTIVATOR II 10/24/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 08/22/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 08/18/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 08/18/2023
BOSTON SCIENTIFIC CORPORATION CAPTIFLEX 07/25/2023
BOSTON SCIENTIFIC CORPORATION CAPTIVATOR 06/12/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 03/01/2023
BOSTON SCIENTIFIC CORPORATION SENSATION SHORT THROW 12/30/2022
BOSTON SCIENTIFIC CORPORATION CAPTIFLEX 12/14/2022
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