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BioWorld - Saturday, June 20, 2026
Home » Authors » Liz Hollis

Liz Hollis

Articles

ARTICLES

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Nevro shines following quarterly results, positive news on NSRBP study

Feb. 26, 2020
By Liz Hollis
Nevro Corp.’s stock was up following encouraging results detailed during its fourth-quarter earnings call. Management predicted a positive 2020, highlighting the potential of the U.S. spinal cord stimulation (SCS) market. Keith Grossman, chair, CEO and president of the company, noted that the SCS market slowed last year as a result of stocking issues – a challenge that affected both it and its competitors.
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FDA clears Novalung, the first ECMO system for long-term use

Feb. 25, 2020
By Liz Hollis
The U.S. FDA has given its nod to Novalung, a heart and lung support system from Fresenius Medical Care North America (FMCNA) for the treatment of acute respiratory or cardiopulmonary failure. The Waltham, Mass.-based company noted that Novalung is the first extracorporeal membrane oxygenation (ECMO) system to be cleared for more than six hours of use.
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BioWorld MedTech’s Cardiology Extra for Feb. 24, 2020

Feb. 24, 2020
By Liz Hollis
Keeping you up to date on recent developments in cardiology, including: Using AI to predict heart attacks, stroke; Startup focuses on nano-capsules derived from milk to deliver heart drug; Biotronik sees positive results with ultrathin strut DES.
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De novo key on keyboard

FDA gives nod to Asuragen’s Amplidex Fragile X Dx and Carrier Screen Kit

Feb. 24, 2020
By Liz Hollis
Asuragen Inc., an Austin, Texas-based molecular diagnostics company, has received good news from the U.S. FDA. The agency gave the green light for the company’s Amplidex Fragile X Dx and Carrier Screen Kit, which aims to detect a genetic condition known as Fragile X syndrome. The diagnostic kit determines the number of cytosine-guanine-guanine (CGG) repeats in the FMR1 gene to aid in the diagnosis of Fragile X syndrome and associated disorders, including Fragile X-associated tremor/ataxia syndrome and Fragile X-associated primary ovarian insufficiency.
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Body scan analysis

Q Bio scores $40M in series B, eyes opening additional centers, enhancing digital health platform

Feb. 21, 2020
By Liz Hollis
Redwood City, Calif.-based Q Bio Inc., which is offering a quantitative assessment of personal health, has come out of stealth mode, scooping up $40 million in a series B funding round led by Andreessen Horowitz. The funds are earmarked to improve its proprietary platform and technology to make its preventive health services faster, better and more affordable for all.
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Trisalus initiates study for delivery tech to help patients with pancreatic tumors

Feb. 20, 2020
By Liz Hollis
Trisalus Life Sciences Inc., of Westminster, Colo., reported the start of a clinical trial assessing a treatment that combines its intravascular, tumor-directed proprietary Pressure-Enabled Drug Delivery (PEDD) approach with standard-of-care systemic chemotherapy.
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Bionano Genomics sees encouraging results from study of Saphyr

Feb. 19, 2020
By Liz Hollis
The results from a study comparing San Diego-based Bionano Genomics Inc.’s Saphyr to traditional cytogenetic methods for the clinical analysis of leukemia genomes revealed that the system was 100% concordant with the standard of care for the detection of somatic chromosomal abnormalities.
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Ribbons of digital data

Sutter Health sees promise with Ferrum's AI quality platform in preventing medical errors

Feb. 18, 2020
By Liz Hollis
Ferrum Health Inc., of San Francisco, is looking to prevent medical errors with the help of artificial intelligence (AI). That caught the eye of Sutter Health, a not-for-profit health care network in Northern California. To that end, the two have unveiled the debut of Ferrum's AI-powered platform as the system to deliver more consistent care to patients.
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Woman giving birth

Alydia Health wraps up enrollment in pivotal study of device postpartum hemorrhage

Feb. 14, 2020
By Liz Hollis
Alydia Health Inc., of Menlo Park, Calif., has completed enrollment in the pivotal PEARLE investigational device exemption (IDE) study, which is assessing the safety and effectiveness of the Jada system to rapidly control and treat abnormal postpartum uterine bleeding and postpartum hemorrhage.
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Bedside MRI system receives green light from the FDA

Feb. 12, 2020
By Liz Hollis
Guilford, Conn.-based Hyperfine Research Inc. has received the U.S. FDA’s nod for a bedside magnetic resonance imaging (MRI) system and is eyeing this summer for shipments. The portable system can be wheeled directly to the patient’s bedside and plugs into a standard electrical wall outlet.
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View All Articles by Liz Hollis

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