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News You Need to Know Today
Comparing popular TAVR valves | Teleflex to acquire Biotronik assets for $791M | FDA sued over semaglutide | Google's good news
Friday, February 28, 2025
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Today's News and Trends

Popular TAVR valves linked to comparable long-term outcomes

Second-generation TAVR valves from Medtronic, Edwards Lifesciences and Boston Scientific are all associated with similar seven-year outcomes, according to a new retrospective study out of Italy. 

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The Medtronic CoreValve Evolut and the Edwards Lifesciences Sapien 3 TAVR valves.
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Popular TAVR valves linked to comparable long-term outcomes

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The Medtronic CoreValve Evolut and the Edwards Lifesciences Sapien 3 TAVR valves.
Second-generation TAVR valves from Medtronic, Edwards Lifesciences and Boston Scientific are all associated with similar seven-year outcomes, according to a new retrospective study out of Italy. 
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Teleflex to acquire Biotronik’s vascular intervention business for $791M, split into 2 separate entities

The acquisition helps Teleflex expand its interventional and vascular portfolios. Biotronik, meanwhile, is shifting its focus toward implantable devices and digital healthcare. 

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Business newspaper
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Teleflex to acquire Biotronik’s vascular intervention business for $791M, split into 2 separate entities

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Business newspaper
The acquisition helps Teleflex expand its interventional and vascular portfolios. Biotronik, meanwhile, is shifting its focus toward implantable devices and digital healthcare. 
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FDA sued over ‘reckless and arbitrary’ semaglutide decision

The Outsourcing Facilities Association, a Texas-based trade group, is alleging that supply issues still remain for Ozempic and Wegovy. The group believes the FDA has ignored those issues.

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FDA sued over ‘reckless and arbitrary’ semaglutide decision

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The Outsourcing Facilities Association, a Texas-based trade group, is alleging that supply issues still remain for Ozempic and Wegovy. The group believes the FDA has ignored those issues.
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FDA clears Google smartwatch tech that calls 911 when a user’s heart stops

Google worked with AI specialists, cardiologists and even stunt performers to develop its new smartwatch feature.

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Google has received U.S. Food and Drug Administration (FDA) for Loss of Pulse Detection, a new smartwatch feature that detects when a person’s heart stops beating and then automatically alerts emergency services. Good Pixel Smartwatch Loss of Pulse.
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FDA clears Google smartwatch tech that calls 911 when a user’s heart stops

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Google has received U.S. Food and Drug Administration (FDA) for Loss of Pulse Detection, a new smartwatch feature that detects when a person’s heart stops beating and then automatically alerts emergency services. Good Pixel Smartwatch Loss of Pulse.
Google worked with AI specialists, cardiologists and even stunt performers to develop its new smartwatch feature.
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Featured Articles

Medtronic enrolls first patient in new coronary DCB trial—data could lead to FDA approval

The paclitaxel-coated device, already approved in Europe and other parts of the world, will be tested on more than 1,200 patients for a new international trial. If the study is a success, Medtronic hopes to gain regulatory approval in the United States and Japan. 

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Prevail DCB Medtronic. Medtronic’s Prevail drug-coated balloon (DCB) has received CE mark approval for several new indications related to the treatment of coronary artery disease (CAD). The paclitaxel-coated device, designed to inflate within the patient’s artery during percutaneous coronary intervention (PCI) procedures, is now approved across the EU to treat CAD patients with multivessel disease, acute coronary syndrome and diabetes.
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Medtronic enrolls first patient in new coronary DCB trial—data could lead to FDA approval

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Prevail DCB Medtronic. Medtronic’s Prevail drug-coated balloon (DCB) has received CE mark approval for several new indications related to the treatment of coronary artery disease (CAD). The paclitaxel-coated device, designed to inflate within the patient’s artery during percutaneous coronary intervention (PCI) procedures, is now approved across the EU to treat CAD patients with multivessel disease, acute coronary syndrome and diabetes.
The paclitaxel-coated device, already approved in Europe and other parts of the world, will be tested on more than 1,200 patients for a new international trial. If the study is a success, Medtronic hopes to gain regulatory approval in the United States and Japan. 
READ MORE >

Detecting coronary inflammation on CT imaging could reshape preventive cardiology

New technology now being considered by the FDA for approval can capture coronary inflammation on CCTA images and provide risk assessments. What could this mean for the future of cardiac care? We spoke to one researcher to learn more.

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Charalambos Antoniades, MD, the British Heart Foundation Chair of Cardiovascular Medicine at the University of Oxford, is a co-founder of the company Caristo, which has developed technology to image coronary inflammation on coronary computed tomography angiography (CCTA) scans to visualize a key factor of residual cardiovascular risk.
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Detecting coronary inflammation on CT imaging could reshape preventive cardiology

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Charalambos Antoniades, MD, the British Heart Foundation Chair of Cardiovascular Medicine at the University of Oxford, is a co-founder of the company Caristo, which has developed technology to image coronary inflammation on coronary computed tomography angiography (CCTA) scans to visualize a key factor of residual cardiovascular risk.
New technology now being considered by the FDA for approval can capture coronary inflammation on CCTA images and provide risk assessments. What could this mean for the future of cardiac care? We spoke to one researcher to learn more.
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‘A significant milestone’: First US patients receive doses of new PET radiotracer for CAD

Back in September, the FDA approved GE HealthCare’s new PET radiotracer, flurpiridaz F-18, for patients with known or suspected CAD. It is seen by many in the industry as a major step forward in patient care. 

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The new cardiac PET radiotracer flurpiridaz F-18 is posed to be a major game changer and will likely lead to increased adoption of cardiac PET.
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‘A significant milestone’: First US patients receive doses of new PET radiotracer for CAD

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The new cardiac PET radiotracer flurpiridaz F-18 is posed to be a major game changer and will likely lead to increased adoption of cardiac PET.
Back in September, the FDA approved GE HealthCare’s new PET radiotracer, flurpiridaz F-18, for patients with known or suspected CAD. It is seen by many in the industry as a major step forward in patient care. 
READ MORE >

Wearable heart device company to go public, raise up to $155M

Kestra Medical Technologies, known for its wearable heart monitors and defibrillators, intends to sell 10 million common shares priced somewhere between $14 and $16 per share. 

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Kestra Medical Technologies
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Wearable heart device company to go public, raise up to $155M

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Kestra Medical Technologies
Kestra Medical Technologies, known for its wearable heart monitors and defibrillators, intends to sell 10 million common shares priced somewhere between $14 and $16 per share. 
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In Case You Missed It

Report: Johnson & Johnson wants to sell its stroke business for more than $1B

Johnson & Johnson has reportedly had early discussions with potential buyers about its Cerenovus division of stroke products.

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artificial intelligence money finance acquisition
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Report: Johnson & Johnson wants to sell its stroke business for more than $1B

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artificial intelligence money finance acquisition
Johnson & Johnson has reportedly had early discussions with potential buyers about its Cerenovus division of stroke products.
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Final decision on the creation of a new cardiovascular board expected soon

U.S. cardiology groups have worked together to propose the creation of a new American Board of Cardiovascular Medicine for certifying cardiologists. Now, after many months of waiting, a final decision is expected by the end of February. 

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ACC Vice President Christopher Kramer, MD, FACC, offers an update on the creation of a new cardiovascular board.
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Final decision on the creation of a new cardiovascular board expected soon

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ACC Vice President Christopher Kramer, MD, FACC, offers an update on the creation of a new cardiovascular board.
U.S. cardiology groups have worked together to propose the creation of a new American Board of Cardiovascular Medicine for certifying cardiologists. Now, after many months of waiting, a final decision is expected by the end of February. 
READ MORE >

Use of biolimus-coated balloons during PCI not as effective as paclitaxel devices

Researchers tracked data from more than 200 patients who underwent PCI from August 2020 to July 2022, sharing their findings in JACC: Cardiovascular Interventions.

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doctor wrong patient wrong-site surgery medical error malpractice mistake
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Use of biolimus-coated balloons during PCI not as effective as paclitaxel devices

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doctor wrong patient wrong-site surgery medical error malpractice mistake
Researchers tracked data from more than 200 patients who underwent PCI from August 2020 to July 2022, sharing their findings in JACC: Cardiovascular Interventions.
READ MORE >

In Other News

Walgreens resolves $595M lawsuit over COVID testing

The dispute was with Everly Health, a telemedicine provider contracted to fulfill orders for COVID-19 tests during the pandemic. Walgreens was accused of violating provisions of a service agreement. 

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Walgreens resolves $595M lawsuit over COVID testing

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The dispute was with Everly Health, a telemedicine provider contracted to fulfill orders for COVID-19 tests during the pandemic. Walgreens was accused of violating provisions of a service agreement. 
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Primary care is primed for AI. But is AI aligned with primary care?

Fewer than one-third of primary care clinicians have a say in selecting the AI products their institutions expect them to fold into their clinical workflows. That’s a problem. 

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primary care provider clinician physician doctor
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Primary care is primed for AI. But is AI aligned with primary care?

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primary care provider clinician physician doctor
Fewer than one-third of primary care clinicians have a say in selecting the AI products their institutions expect them to fold into their clinical workflows. That’s a problem. 
READ MORE >

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