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Lucira Health, Inc. was a medical technology company focused on the development and commercialization of innovative infectious disease test kits. The company gained prominence for producing the first FDA-authorized at-home molecular COVID-19 test and later, a combined COVID-19 & Flu home test. In February 2023, Lucira Health filed for Chapter 11 bankruptcy and its assets were subsequently acquired by Pfizer Inc., with the acquisition formally announced as agreed in April 2023 and completed later that year. Prior to its acquisition, Lucira aimed to transform community-based healthcare by providing accessible, user-friendly, and accurate diagnostic solutions directly to consumers and healthcare providers.
The Emeryville headquarters served as the primary center for Lucira Health's operations, including research and development of its diagnostic tests, corporate administration, regulatory affairs, and commercial strategy prior to its acquisition.
The facility was equipped with necessary laboratory infrastructure for molecular diagnostic R&D and quality control, alongside office spaces. Specific unique architectural highlights were not a primary public focus of the company.
As a health-tech company developing critical diagnostics during a pandemic, Lucira Health's work culture was likely characterized by a strong sense of mission, innovation, and urgency. It would have attracted individuals dedicated to public health and scientific advancement, operating in a dynamic, fast-paced environment typical of biotech firms in the Bay Area.
The Emeryville headquarters was significant as the operational base where Lucira Health developed and brought to market pioneering at-home diagnostic solutions, notably the first FDA-authorized at-home molecular COVID-19 test and a combined COVID-19 & Flu test. It represented a key site for innovation in decentralized medical testing.
Prior to its acquisition by Pfizer, Lucira Health had established a growing global presence. While its primary market was the United States, the company secured regulatory approvals and initiated commercialization for its at-home diagnostic tests in several international regions. This included Health Canada authorization, the CE Mark in Europe allowing access to EU markets, and approvals/distribution in countries such as Singapore, Taiwan, and Israel. This expansion was supported through direct efforts and strategic partnerships to make their tests available globally.
1412 62nd Street
Emeryville
California
USA
Address: Leased warehouse space; specific street address not publicly detailed, facility located in Hayward, California.
To manage inventory, packaging, and shipment of products, ensuring timely delivery across the United States and to other markets where their products were authorized.
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As of April 2025, Lucira Health' leadership includes:
Lucira Health has been backed by several prominent investors over the years, including:
In the year leading up to its Chapter 11 filing in February 2023, Lucira Health experienced at least one notable C-level executive departure. The primary leadership team otherwise remained focused on product development and navigating market challenges. The most significant 'exits' for the entire executive team occurred as a consequence of the bankruptcy and subsequent acquisition by Pfizer in early-mid 2023.
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Historically, Lucira Health likely utilized standard corporate email formats such as [first_initial][last]@lucirahealth.com. Following its acquisition by Pfizer and cessation of independent operations, these email addresses are no longer active. For inquiries regarding former Lucira Health products, please refer to Pfizer's official communication channels.
[first_initial][last]@lucirahealth.com (e.g., jsmith@lucirahealth.com)
Format
asmith@lucirahealth.com
Example
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Success rate
Pfizer News • April 6, 2023
Pfizer Inc. announced it had entered into a definitive agreement to acquire Lucira Health, Inc. The transaction, which followed Lucira's Chapter 11 bankruptcy filing, aimed to enhance Pfizer's portfolio of diagnostic tests for infectious diseases, including Lucira's FDA-authorized COVID-19 and flu home test....more
U.S. Food and Drug Administration (FDA) • February 24, 2023
The U.S. FDA granted Emergency Use Authorization (EUA) for Lucira Health's COVID-19 & Flu Home Test. This was the first over-the-counter at-home diagnostic authorized to detect Influenza A, Influenza B, and SARS-CoV-2 from a single self-collected nasal swab. This authorization occurred shortly after Lucira filed for Chapter 11 bankruptcy....more
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