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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 10/28/2022
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 10/19/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM ASD OCCLUDER 09/27/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 09/27/2022
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 09/20/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 09/14/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 08/31/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 08/31/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 08/26/2022
W. L. GORE & ASSOCIATES, INC. GORE® CARDIOFORM SEPTAL OCCLUDER 08/24/2022
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