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Data / Medical devices / Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation / United States

FDA-registered makers of Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation (product code OCM). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
Product code
OCM
Country
United States

Makers of Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Atricure, Inc.Mason, OH, United StatesComplaint file establishment, Manufacturer, Specification developer0200api.fda.gov
Cardiofocus, Inc.Marlborough, MA, United StatesManufacturer for export0000api.fda.gov
Minnetronix, Inc.Saint Paul, MN, United StatesContract manufacturer0000api.fda.gov
Stellartech Research Corp.Milpitas, CA, United StatesContract manufacturer0000api.fda.gov
VestaFranklin, WI, United StatesContract manufacturer0000api.fda.gov
Xeridiem Medical DevicesTucson, AZ, United StatesContract manufacturer0000api.fda.gov

Updated November 3, 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.