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BioWorld - Friday, January 16, 2026
Home » Topics » Medical devices and technologies » Medical devices

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French flags on building

Med-tech companies in France suffering from regulatory inertia in their home market

Feb. 25, 2020
By Bernard Banga
PARIS – The Syndicat National de l'Industrie des Technologies Médicales (SNITEM), the French national association of medical technology manufacturers, has just released a study looking at the development of this industrial sector in that country. This snapshot, produced every two years by the firm D&Consultants SAS on behalf of Courbevoie, France-based SNITEM and the bank Bpifrance SA, is based on a dual quantitative and qualitative approach.
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Australian flag on laptop screen with health professional

Australia lays out evidence requirements for device marketing authorization applications

Feb. 20, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has issued a draft guidance to help sponsors better understand the evidence requirements for market authorizations for medical devices, including in vitro diagnostics (IVDs) and software as a medical device (SaMD).
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1-17-Novocure-Optune-Device

Novocure revenue climbs 42% to $99.2M in 2019 fourth quarter

Jan. 17, 2020
By Meg Bryant
Novocure Ltd. of St. Helier, Jersey, released preliminary fourth-quarter and full-year 2019 results, showing strong momentum with its tumor treating fields (TTF) technology, a noninvasive, antimitotic therapy delivered via the Optune device. Q4 revenue is expected to hit $99.2 million, up 42% from $69.7 million in the same period last year, with anticipated full-year revenue of $351.3 million, also up 42%. In the U.S., net revenues grew 49% to $65.9 million in the last financial quarter.  
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Gavel and scales

DC district court hands FDA a product jurisdiction loss in barium sulfate suit

Dec. 10, 2019
By Mark McCarty
The FDA has lost a product jurisdiction case in DC district court to Genus Medical Technologies LLC over its barium sulfate contrast agent. The judge in the case ruled that the agency violated the Administrative Procedures Act in ruling that the product is a drug, but the FDA will have another crack at the matter as the application for the product has been remanded to the FDA.
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Ancora Heart sees positive early results with Accucinch in systolic heart failure

Sep. 30, 2019
By Liz Hollis

Shockwave reports positive registry data on pre-stent calcium fracture via IVL

Sep. 27, 2019
By Stacy Lawrence
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