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BioWorld - Tuesday, February 10, 2026
Home » Topics » U.S., Medical technology

U.S., Medical technology
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Testing being performed on Abbott's ID Now system

Abbott pushes back on Langone study of ID Now test; FDA cites possibility of swab, transport media issues

May 15, 2020
By Mark McCarty
Abbott Laboratories’ ID Now test for the SARS-CoV-2 virus made waves when it was introduced thanks to the rapid turnaround time the molecular test promised. But questions about the test’s performance have surfaced several times in recent weeks. The latest criticism comes from a study conducted at the New York University Langone Medical Center, which claims the diagnostic compared poorly against a competitor. However, the U.S. FDA said that it has questions about the swabs and transport media used in connection with the test. As a result, it will stand pat regarding the ID Now’s place in the emergency use authorization (EUA) program.
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Richard Bright testifying before House subcommittee

Bright warns of ‘darkest winter in modern history’

May 14, 2020
By Mari Serebrov
“Our window of opportunity is closing. If we fail to develop a national coordinated response, based in science, I fear the pandemic will get far worse and be prolonged, causing unprecedented illness and fatalities,” Rick Bright, former director of the Biomedical Advanced Research and Development Authority, said today as he testified at a House subcommittee hearing on the U.S. response to COVID-19.
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Surgeon using the ORlenz headset

Ocutrx debuts AR-based system for surgical visualization

May 14, 2020
By Meg Bryant
Irvine, Calif.-based startup Ocutrx Vision Technologies LLC unveiled new technology that it said helps surgeons better visualize the operative field during surgical procedures. The OR-Bot Surgery Visualization Theatre combines augmented reality (AR), virtual reality (VR) and both human- and robot-controlled arms to facilitate exacting medical procedures without the need for physicians to look away from the patient.
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Patent gears

PTO offers priority for pandemic-related patents, but time of the essence

May 14, 2020
By Mark McCarty
The U.S. Patent and Trademark Office (PTO) has opened a priority track for patents related to the COVID-19 pandemic, another signal of federal government intent on overcoming this new plague. However, Scott Marty, a partner with the Atlanta office of Ballard Spahr LLP, told BioWorld that while the program offers some distinct advantages for pandemic-driven patents, inventors should have their filings in good form before entry because any delays incurred by a less-than-airtight application could lead the PTO to boot the application out of this program.
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Physician using an Ipad

Nanthealth looks to help cancer patients during pandemic

May 13, 2020
By Liz Hollis
How is the COVID-19 pandemic affecting cancer treatment plans? Oncologists are weighing switching treatment plans, and they have many questions. That’s where Nanthealth Inc., of El Segundo, Calif., is looking to help.
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Digital illustration of U.S., coronavirus
World Medical Innovation Forum

U.S. COVID-19 Dx: Lack of centralization meets flourishing innovation, as disorder prevails

May 13, 2020
By Stacy Lawrence
The U.S. does not have a universal health care system, which means that it fails to provide a consistent level of minimum care across its population. That means that basic and preventative care often falls through the cracks, even as the U.S. continues to excel at medical innovation and offer the most highly regarded health care in the world to those who can afford it.
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HD-X system

Quanterix says COVID-19 antibody test with Simoa platform has 1,000x greater sensitivity than current tests

May 12, 2020
By Meg Bryant
Quanterix Corp., of Billerica, Mass., reported that researchers have developed a COVID-19 antibody test with 1,000 times the sensitivity of current tests using its Simoa bead-based immunoassay platform.
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Propel implant devices

COVID-19 hits Intersect ENT after good start to year

May 12, 2020
By Liz Hollis
Intersect ENT Inc., of Menlo Park, Calif., saw its revenue for the first quarter of 2020 fall to $19.8 million. That figure compares with $26.7 million for the same period last year, with the COVID-19 pandemic having a significant impact on procedures.
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NIAID Director Anthony Fauci speaking at a White House briefing

Fauci ‘cautiously optimistic’ regarding COVID-19 vaccine; Giroir projects 50M tests per month by September

May 12, 2020
By Mark McCarty
The May 12 Senate hearing regarding the COVID-19 pandemic included the usual conversations about contact tracing, but Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, said he is “cautiously optimistic” that one of the vaccines currently in trial in the U.S. will work, but that it is unlikely a vaccine will be ready by September 2020. In contrast, Assistant Secretary for Health Brett Giroir said testing capacity may reach 50 million tests per month by that time, thanks in part to the fact that antigen testing is now part of the FDA’s emergency use authorization mechanism.
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Digital illustration of U.S., coronavirus

FTC active in litigation over advertising, promotional claims during pandemic

May 8, 2020
By Mark McCarty
The U.S. FDA’s enforcement regarding products related to the COVID-19 pandemic has picked up steam recently, but the U.S. Federal trade commission (FTC) is also involved in this enforcement arena. Leonard Gordon, a partner at Venable LLP’s New York office, told BioWorld that while the FTC and FDA missions seem to overlap, the FTC primarily targets unsupportable advertising claims rather than product labeling, a particularly relevant area in the COVID-19 pandemic.
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