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Data / Medical devices / System, Appendage Closure, Left Atrial / United States

FDA-registered makers of System, Appendage Closure, Left Atrial in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make System, Appendage Closure, Left Atrial (product code NGV). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.

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Device
System, Appendage Closure, Left Atrial
Product code
NGV
Country
United States

Makers of System, Appendage Closure, Left Atrial in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Abbott MedicalPlymouth, MN, United StatesManufacturer0100api.fda.gov
Abbott MedicalSaint Paul, MN, United StatesSpecification developer0100api.fda.gov
Boston Scientific CorporationMaple Grove, MN, United StatesSpecification developer0110api.fda.gov
Boston Scientific Corp., Marina Bay Cust. Fulfillment CenterQuincy, MA, United StatesManufacturer0100api.fda.gov
Boston Scientific CorporationCoventry, RI, United StatesManufacturer0100api.fda.gov
St. Jude MedicalRoseville, MN, United StatesManufacturer0100api.fda.gov
St. Jude Medical, Cardiology Division, Inc.Plymouth, MN, United StatesManufacturer for export0010api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.