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NEW YORK – Binx Health said on Thursday it has received a second 510(k) clearance from the US Food and Drug Administration for the Binx io molecular point-of-care platform for the detection of chlamydia and gonorrhea in male urine specimens.

The agency cleared the system in August 2019 for use with clinician and self-collected vaginal swab specimens.

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A survey by Nature finds that most researchers want scientific meetings to continue virtually or with a virtual component, even after the pandemic ends.

Bloomberg reports that the B.1.351 SARS-CoV-2 viral variant could prompt the formulation of better vaccines.

Certain blood proteins may be able to distinguish COVID-19 patients who will become critically ill from those who will not, the Atlanta Journal-Constitution reports.

In Genome Biology this week: algorithm to assess regulatory features, approach to integrate multiple single-cell RNA-seq datasets, and more.