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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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56 records meeting your search criteria returned- Product Code: MLV Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE® CARDIOFORM ASD OCCLUDER 02/05/2020
W.L. GORE & ASSOCIATES GORE HELEX SEPTAL OCCLUDER 12/03/2019
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 10/16/2019
W.L. GORE & ASSOCIATES GORE HELEX SEPTAL OCCLUDER 01/10/2019
W.L. GORE & ASSOCIATES GORE CARDIOFORM SEPTAL OCCLUDER 11/06/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 07/25/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 05/23/2018
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 11/06/2017
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 08/30/2017
W.L. GORE & ASSOCIATES GORE® CARDIOFORM SEPTAL OCCLUDER 11/11/2015
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