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BioWorld - Saturday, February 21, 2026
Home » Topics » U.S., Medical technology

U.S., Medical technology
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Device in heart

Patient selection rules the day in study of TAVR at centers with SAVR

Feb. 7, 2020
By Mark McCarty
The advent of transcatheter aortic valve replacement (TAVR) changed the framework for dealing with aortic valve stenosis, but some clinicians might argue there was a corresponding and inappropriate rush away from surgical aortic valve replacement (SAVR).
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Nanospectra launches pivotal trial of Aurolase therapy

Feb. 7, 2020
By Meg Bryant
Houston-based Nanospectra Biosciences Inc. has kicked off a pivotal U.S. study of its Aurolase therapy in the targeted destruction of prostate tumors using nanomedicine technology. The IDE study, with an estimated completion date of December 2022, will support a de novo 510(k) submission to the U.S. FDA. The first two patients were treated at the University of Michigan, which also participated in the first-in-human pilot study of Aurolase.
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Device warnings resurgent despite FDA’s claim Theranos discovery a distraction

Feb. 6, 2020
By Mark McCarty
FDA warning letters to device makers have been conspicuous in their paucity in recent years, but they have been surfacing with greater frequency over the past few months.
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Dollar sign, downward arrow

BD lowers 2020 guidance, stock drops 13% on news of Alaris regulatory holdup

Feb. 6, 2020
By Meg Bryant
Becton, Dickinson and Co. (BD) (NYSE:BDX) reported revenue of $4.23 billion for the first quarter of fiscal year 2020, ended Dec. 31, up 1.6% from the same period a year ago. Revenue grew 2.5% on a currency-neutral basis. However, an unexpected regulatory hurdle for its Alaris infusion pumps caused the Franklin Lakes, N.J.-based company to lower its 2020 revenue and earnings guidance. Despite the shadow cast by the Alaris news, BD beat Street expectations for the quarter – clocking in at $4.23 billion vs. $4.18 billion.
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Medicare puzzle

Abbott urges CMS to rethink coverage for ventricular assist devices

Feb. 5, 2020
By Mark McCarty
Medicare coverage of ventricular assist devices assumes the patient is either in end-stage heart failure or could become a candidate for transplant, but that approach may soon change. Abbott Laboratories, of Abbott Park, Ill., has asked that Medicare coverage assume the patient can recover myocardial function, a paradigm shift that is backed by clinical evidence.
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Pills in dollar sign, bottle, blister packs, money

Congress must do the seemingly impossible – seek bipartisan solutions

Feb. 5, 2020
By Mari Serebrov
Touting the efforts his administration already has taken to lower U.S. prescription drug prices through increased competition, President Donald Trump placed the burden for further action squarely on Congress during his State of the Union address Tuesday, Feb. 4.
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Preventing a U.S. outbreak: Emergency declaration leads to hunt for more funding

Feb. 4, 2020
By Mari Serebrov
Now that U.S. Health and Human Services (HHS) Secretary Alex Azar has declared a nationwide public health emergency due to the 2019 novel coronavirus (2019-nCoV), HHS is saying it may need more money to help it be as proactive and aggressive as possible in detecting the virus and containing an outbreak.
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Blue heart and data grid

CMS eyes Syncardia petition to drop CED for artificial hearts

Feb. 4, 2020
By Mark McCarty
Syncardia Systems LLC, of Tucson, Ariz., has petitioned the Centers for Medicare and Medicaid Services (CMS) to drop the coverage with evidence development (CED) mandate for artificial hearts, stating that multiple studies have demonstrated that artificial hearts meet the reasonable and necessary standard. Syncardia said its temporary Total Artificial Heart (TAH-t) should thus be available “unencumbered by the existing requirement for evidence development,” a change that could modestly bolster utilization and sales of these devices.
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Business, data, dollars illustration

Zimmer Biomet sees results that exceeded expectations with knees, hips standing out

Feb. 4, 2020
By Liz Hollis
Zimmer Biomet Holdings Inc., of Warsaw, Ind., reported good news for the fourth quarter, which saw net sales of $2.126 billion, an increase of 2.6% over the prior year period. In terms of geography, the Americas and Asia-Pacific stood out. In addition, the company witnessed strong results globally in its knee and hip businesses.
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2-3-Azar-HHS.png

HHS declares public health emergency in part because CDC test for coronavirus unreliable

Feb. 3, 2020
By Mark McCarty
The U.S. Department of Health and Human Services has declared a public health emergency in the U.S. over the coronavirus in part because a government diagnostic for the virus yields inconsistent results, a fact that may spur the life sciences to provide a solution.
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