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BioWorld - Saturday, January 17, 2026
Home » Topics » Regulatory, BioWorld MedTech

Regulatory, BioWorld MedTech
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Cardiacsense obtains CE mark for atrial fibrillation detection

Feb. 16, 2021
By Annette Boyle
Cardiacsense Ltd.’s medical watch received CE mark for the detection of atrial fibrillation and heart rate variability monitoring. The watch provides continuous, long-term monitoring of heart arrhythmias without cumbersome external devices or invasive implants. The European clearance does not require a prescription for use and will enable the Caesarea, Israel-based company to begin distribution under a number of agreements the company signed in 2020.
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Illustration of vascular system in the legs

Soundbite Medical device for treatment of CTOs approved in Canada

Feb. 16, 2021
By David Godkin
TORONTO – Soundbite Medical Solutions Inc. has received Health Canada approval for a shock wave device that jackhammers its way through calcified, chronic total occlusions (CTO) in life-threatening critical limb ischemia (CLI), a severe form of peripheral artery disease. This comes after the Active Wire 0.014” was used for the first time in late January to successfully treat five patients.
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Illustration of calcified artery, heart

Shockwave Medical gets FDA nod for intravascular lithotripsy for heart disease

Feb. 16, 2021
By Meg Bryant
Shockwave Medical Inc. said Tuesday that its intravascular lithotripsy (IVL) therapy has won U.S. FDA approval for the treatment of severe coronary artery disease (CAD). The technology, which was granted breakthrough device designation in 2019, is a novel application of lithotripsy, which has long been used to safely shatter kidney stones.
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Regulatory front for Feb. 16, 2021

Feb. 16, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Shuren, Stenzel push back on serology tests; FDA touts accomplishments for 2020; IMDRF posts five-year plan.
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Regulatory actions for Feb. 16, 2021

Feb. 16, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Axonics, Electrocore, Front Line Medical Technologies, Insightec, Luminostics, Saladax, Shockwave Medical, Smart Medical.
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COVID-19 vaccine vials behind U.S. capitol building
Pfizer, Moderna agree to deliver 200M more doses

House committee inks spending package for COVID-19 pandemic

Feb. 12, 2021
By Mark McCarty
The U.S. House Energy and Commerce Committee needed two days of hearings to get through a spending measure that provided the FDA with $500 million for its part in the government response. The CDC would receive $7.5 billion for vaccine distribution and tracking, all developments that ran parallel to an announcement that another 200 million doses of vaccine will be delivered by the end of July at a cost of $3.7 billion.
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Mask with Brazilian flag

Seegene strengthens footprint in Latin America via COVID testing

Feb. 12, 2021
By Gina Lee and Sergio Held
COLOMBIA – South Korea’s molecular diagnostics firm Seegene Inc. is expanding operations in the Brazilian market after Anvisa, the country's health care surveillance agency, cleared its multi-assay product through a COVID-19 emergency pathway. Seegene manufactures Allplex, a SARS-CoV-2/FluA/FluB/RSV test able to screen and differentiate eight targets.
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Braincool wins breakthrough nod for system to prevent painful chemo side effect

Feb. 12, 2021
By Meg Bryant
Braincool AB has scored a breakthrough device designation from the U.S. FDA for its Cooral system, a medical cooling technology for therapeutic hypothermia and oncology. The status acknowledges Cooral’s potential to prevent oral mucositis (OM), a complication of chemotherapy.
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Regulatory front for Feb. 12, 2021

Feb. 12, 2021
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA cites pivotal study failure for Lutonix 014; HHS adds to PREP Act immunity; Dermal fillers on tap at FDA advisory; GAO urges a pause in VA EHR deployment.
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Regulatory actions for Feb. 12, 2021

Feb. 12, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Becton Dickinson.
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