Rheonix
FDA Emergency Use Authorization for Rheonix SARS-CoV-2 Assay Expanded to Include Saliva Samples
The expanded EUA allows for testing of saliva samples collected in a sterile tube in a hospital setting.
Rheonix Gets FDA Emergency Use Authorization for Coronavirus MDx Test
The endpoint RT-PCR test is processed on the company's Encompass CARD cartridge, which runs on Rheonix's Encompass MDx workstation.
Commercial Coronavirus Test Developers Tweak Timelines, EUA Plans in Light of Loosened FDA Guidance
Test makers are preparing to ramp up production of new SARS-CoV-2 assays and designated testing systems in anticipation of increased demand.
Coronavirus Dx Emergency Use Authorizations Progressing Rapidly Despite Criticism
SARS-CoV-2 viral material is available for test validation, and the FDA is conducting a rolling review process with an abbreviated submission template.
Oct 15, 2015
Rheonix Raises $28.6M
May 27, 2015
Oct 7, 2014
May 13, 2014
Feb 13, 2014
Feb 11, 2014
Dec 17, 2013
Rheonix Raises $14M in Private Financing
Dec 17, 2013