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LMDX News and Press, LumiraDx Limited From 03/21/23

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Company Name: LumiraDx Limited
Stock Symbol: LMDX
Market: NASDAQ

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LMDX - LumiraDx Reports Fourth Quarter and Full Year 2022 Results

LONDON, March 21, 2023 (GLOBE NEWSWIRE) -- LumiraDx Limited (NASDAQ: LMDX), a next-generation point of care (POC) diagnostics company, today announced financial results for its fourth quarter and full year ended December 31, 2022. Full year 2022 revenues of $254.5 million. Q4 2022 reven...

LMDX - LumiraDx to Announce Fourth Quarter and Full Year 2022 Financial Results and Host Quarterly Conference Call on March 21

LONDON, March 14, 2023 (GLOBE NEWSWIRE) -- LumiraDx Limited (Nasdaq: LMDX), a next-generation point of care (POC) diagnostics company, announced it will release its fourth quarter and full year 2022 financial results on Tuesday, March 21 st , 2023. On the day of the release, LumiraD...

LMDX - LumiraDx to Present at Raymond James Institutional Investors Conference

LONDON, March 03, 2023 (GLOBE NEWSWIRE) -- LumiraDx Limited (Nasdaq: LMDX) (the “Company”) today announced that Chief Financial Officer, Dorian LeBlanc, will be presenting at the Raymond James Institutional Investors Conference on Tuesday, March 7 th , 2023 at 4:35pm ET. Webcast...

LMDX - LumiraDx Regains Compliance with Nasdaq Continued Listing Requirements

LONDON, Feb. 17, 2023 (GLOBE NEWSWIRE) -- LumiraDx Limited (Nasdaq: LMDX) (the “Company”) today announced that it has received confirmation from The Nasdaq Stock Market LLC (“Nasdaq”) that it has regained compliance with the minimum bid price requirement under Nasdaq L...

LMDX - LumiraDx wins U.S., U.K. nod for COVID/flu assay

LumiraDx Limited ( NASDAQ: LMDX ) added ~9% pre-market Monday after announcing U.S. and U.K. regulatory clearances for a diagnostic assay that allows the simultaneous detection of COVID-19 and influenza viruses. With the Emergency Use Authorization (EUA) by the FDA and validation ...

LMDX - LumiraDx Receives FDA Emergency Use Authorization and UK CTDA Approval for its Fast Lab Solutions Multiplex COVID and Influenza Molecular Assay

LumiraDx SARS-CoV-2 & Flu A/B RNA STAR Complete assay receives Emergency Use Authorization from the FDA along with being successfully validated by the UK Health Security Agency (UKHSA) under the Coronavirus Test Device Approvals (CTDA) process. This multiplex test utilizes the in...

LMDX - LumiraDx receives non-compliance notice from Nasdaq

LumiraDx ( NASDAQ: LMDX ) said it had received notification from the Nasdaq that it is not in compliance with the minimum bid price  for continued listing as the closing bid price  was below US$1. The Company has a period of 180 calendar days, or until  January 27, ...

LMDX - LumiraDx Announces Commercial Shipment of its Point of Care NT-proBNP Test in Europe, Supporting Heart Health Checks in UK

Run on the highly portable LumiraDx Platform, the LumiraDx NT-proBNP test is a quantitative, fingerstick blood assay designed for near-patient testing with lab-comparable results in 12 minutes. It is the only fingerstick NT-proBNP test currently commercially available. The LumiraDx NT-proBNP ...

LMDX - LumiraDx Announces Receipt of Nasdaq Notification Letter Regarding Minimum Bid Price Deficiency

LONDON, Jan. 31, 2023 (GLOBE NEWSWIRE) -- LumiraDx Limited (Nasdaq: LMDX)(the “Company”) today announced that it has received notification (the “Notification”) from The Nasdaq Stock Market LLC that it is not in compliance with the minimum bid price requirement in Nasda...

LMDX - Latest Clinicians' U.S. Survey Identifies Point of Care Testing (POCT) as a Way to Address Healthcare Bandwidth Pressures and Anticipates Future Growth of POCT in Community Testing Centers

WALTHAM, Mass., Dec. 08, 2022 (GLOBE NEWSWIRE) -- LumiraDx Limited (Nasdaq: LMDX), a next-generation point of care diagnostics company, today announced findings from its second annual “Point of Care Diagnostics: A Clinician's View” U.S. survey, designed to understand physicians...

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