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Quidel Ortho

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San Diego
United States

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Discovers develops, manufactures and markets point-of-care, rapid diagnostic tests for the detection of infectious diseases.

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FDA Authorize At-Home SARS-CoV-2 Rapid Antigen Lateral-Flow Test
Posted: Mar 01, 2021
FDA Authorizes Point-of-Care Rapid Antigen Test for COVID-19 & Influenza A/B
Posted: Oct 16, 2020
Quidel Receives Amended FDA-EUA for Rapid Antigen COVID-19 Diagnostic Assay 
Posted: Jun 18, 2020
Fully-Automated VITROS® Systems Run 150 COVID-19 Blood Tests per Hour
Posted: Apr 14, 2020
FDA Cleared Detection of Borrelia burgdorferi from Finger-Stick Whole Blood Specimens
Posted: Sep 18, 2018
Qualitative Detection and Differentiation of Bordetella pertussis and B. parapertussis
Posted: Jul 24, 2018
FDA Clearance for QuickVue® Influenza A+B Test
Posted: Feb 20, 2018
FDA Clearance for Solana® C. difficile Molecular Assay
Posted: May 30, 2017
FDA Clearance for Solana® Strep Complete Assay
Posted: Nov 01, 2016
FDA Clearance for Quidel's Solana® Influenza A+B Assay
Posted: Oct 04, 2016
A Hand-Held Molecular Diagnostic Test for Trichomoniasis - FDA Cleared
Posted: Apr 07, 2015
FDA Clearance and CLIA Waiver for Strep A FIA
Posted: Jan 05, 2015
Hand-Held Molecular Diagnostic Test for Group A Strep
Posted: Sep 01, 2014
Real-time PCR Assay for HSV 1+2 and VZV gets FDA Clearance
Posted: May 15, 2014
AmpliVue® Hand-Held Molecular Diagnostic Test for HSV Types 1 and 2
Posted: Apr 01, 2014
FDA Clearance for Quidel RSV and hMPV Molecular Tests
Posted: Mar 26, 2013
FDA Clearance for Quidel AmpliVue® Hand-Held C.difficile Assay
Posted: Dec 18, 2012
Quidel Gets CE Mark for Sofia® Legionella Fluorescent Immunoassay
Posted: Nov 13, 2012
CE Mark for Quidel Direct Specimen Rapid PCR Test for Toxigenic C. difficile
Posted: Aug 06, 2012
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  • C/O O’Mahony Donnelly Limited (Xeinadin Group), BLDG G West Cork Technology Park, Clonakilty, CORK, Ireland P85 VF62.
  • +[353] 2388 31884
  • info@rapidmicrobiology.com

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