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By July 10, 2022July 18th, 2022Medical Animation

What You Should Know About the Aria CV Device

aria cv

You might have heard of the Aria CV device to treat pulmonary arterial hypertension. If you are considering getting the device, here are some facts you should know. Despite the device’s success rate, you need to understand the risks associated with it. You should know about the risks associated with the Aria CV device before you decide to use it. You should also know how it works to treat tachyarrhythmia.

Pulmonary Arterial Hypertension _ Aria CV

The Aria CV PH System is a novel implantable medical device, designed to restore the compliance of pulmonary arteries and help patients manage a progressive disease like PAH. The FDA has given this technology breakthrough device designation. This device helps patients with PAH. Improving their quality of life while reducing their cardiac workload and blood pressure. The device has minimal side effects, which is good news for patients.

The heart pump that Aria CV uses to treat pulmonary arterial hypertension is a right ventricular assist device. This device uses a combination of a right atrial-ventricular assist device to control the pressure inside the heart. The company Aria CV Inc. both made the Impella RP and the Aria CV. These two companies have a long history of research and development, which makes their products cutting-edge and highly effective.

Patients with pulmonary arterial hypertension (PAH) approve of the use of this device. The Central Screening Committee and the Patient Care Team approved the device at the investigation site. It mimics the function of healthy blood vessels. It also helps patients with PAH improve their overall quality of life and extend their lives. The device’s design is to implant the main pulmonary artery. Ultimately, patients with the disease could benefit from its success.

Device For Treating Pulmonary Arterial Hypertension

The company behind the ARIA CV device for treating pulmonary arterial artery disease recently received a breakthrough device designation from the FDA. The device reverts the pulmonary arteries to their normal, elastic state, reducing pressure and increasing blood flow. The company’s goal is to improve the quality of life for patients suffering from PAH. The company is currently in the process of designing the clinical trial for this new device.

The Aria CV device was first implanted in a human patient in Vienna, Austria. After a one-hour implant, the patient experienced reduced blood pressure and improved cardiac output. Patients with IPAH often experience symptoms despite being on medical therapy. This procedure was shown to improve patients’ quality of life and their overall health. ARIA CV is intended for adult patients with World Health Organization Group I pulmonary arterial hypertension who have failed to respond to conventional methods.

After receiving approval for the device, the FDA granted the company an IDE (Investigational Device Exemption) for a pilot study. The company has now developed a device that uses non-focused ultrasonic energy to denervate nerves in the pulmonary vasculature. ARIA CV is currently the only device approved by the FDA to treat PAH. To mimic the natural flow of the pulmonary artery is the inspiration for The company’s device’s design .

Risks Of Aria Cv

The information on Aria CV websites may contain forward-looking statements. These statements may not be accurate, complete, or suitable for your particular situation. While Aria CV endeavors to keep the information current, it disclaims any warranty or representation regarding the accuracy or suitability of any of its information, products, or services. In addition, the website may not be available in all markets or be subject to different regulatory practices.

The company that operates Aria CV is based in St. Paul, Minnesota, and has its principal place of business at 2300 Myrtle Avenue, Suite 250. The company’s website may change its terms of use from time to time. To protect yourself, you should check them frequently before you provide any information. The information on Aria’s CV website is subject to change without notice. Aria CV, Inc. will post any changes to its terms of use on its website.

Users of the website must agree to not disrupt or abuse the website or its security. Furthermore, they must refrain from uploading or distributing any harmful files. Additionally, its website does not permit users to seek or provide specific medical advice or treatment. If you encounter any problems or concerns while using Aria CV, please contact us immediately. You can visit our legal department if you have any questions or concerns about our terms.

Device’s Effectiveness

The FDA has recognized ARIA CV’s pulmonary hypertension system, which can alleviate the symptoms of pulmonary arterial hypertension, a potentially fatal disease. Using an elastic pulmonary artery, this system helps reduce the workload on the heart’s muscles, improves blood flow, and potentially improves the quality of life for patients with PAH. The company’s founders, Drs. John Scandurra and Karl Vollmers, have developed a novel device concept for treating PAH. After testing prototypes on animals, they founded Aria CV, Inc.

The company is advancing the device in a US clinical trial to assess its efficacy. ARIA is developing a fully implantable medical device that mimics the pulmonary artery’s natural function to improve compliance in patients with pulmonary arterial hypertension. The FDA approval of the device in the US expects to reduce the costs of treatment and improve patient access through the new CMS reimbursement pathway.

Although the company has raised $19 million in venture capital, it is still working to develop the technology. The company has only seven employees and relies on contractors to produce the device. However, its progress is encouraging. Aria CV is working to develop a device that can potentially fill a billion-dollar market niche. There are many unknowns about the device’s effectiveness. The company’s success will depend on how well it can demonstrate its effectiveness.

FDA Approval

ARIA CV has received FDA approval for its pulmonary hypertension device. This device is being developed by a medical device company based in Saint Paul, Minnesota. The device has completed a first-in-human clinical study in Vienna and is now preparing for a clinical trial in the United States. It is designed to improve the flow of blood throughout the lungs and reduce cardiac workload, which would result in improved quality of life. The company is currently conducting a trial to assess the long-term use of the device in patients suffering from pulmonary artery hypertension.

There are several contraindications for the Aria CV device, including pre-existing medical conditions. This device may interfere with other medical devices, such as prosthetic cardiac devices or defibrillators. It also may interfere with the function of certain devices inside the heart, such as inferior vena cava filters. This study excludes some patients because they are on immunosuppressive drugs. Aria CV devices do not associate with these contraindications.


Unlike other devices that use batteries, the Aria CV works with a special medical balloon that is inserted into the pulmonary artery. By restoring arterial elasticity, the device lessens the workload on the heart, allowing more natural blood flow. The balloon is powered by a heartbeat, so it will not drain the battery and will be replaced if you stop using it. The device is expensive, but the benefits far outweigh the costs.

10 years ago, the University of Minnesota licensed the Aria CV Pulmonary Hypertension System. The device is meant to help relieve the symptoms of PAH and reduce the abnormal workload placed on the right heart. The effectiveness of these treatments for PAH and extending patients’ lives is expected to improve. However, clinical trials need to test this hypothesis. The device costs are expected to vary significantly, and they will likely remain high despite the promising results so far.

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