27 June 2025.
Atmo Biosciences is delighted to announce that it has received US Food and Drug Administration (FDA) 510(k) clearance for the Atmo Gas Capsule System, paving the way for its first product to be marketed and sold in the USA.
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March 4, 2025.
Today, Atmo Biosciences announced the publication of pivotal clinical study data in Clinical Gastroenterology and Hepatology. The study validates the Atmo Capsule for assessing whole and regional gastrointestinal transit times to assist with the diagnosis of motility disorders such as gastroparesis and slow transit constipation.
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April 9, 2024.
Atmo Biosciences is delighted to report that it has successfully reached its primary endpoints in a pivotal clinical study to assess whole and regional gut transit time in subjects with suspected gastrointestinal motility disorders.
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December 14, 2023.
Atmo Biosciences has reached its patient recruitment target ahead of schedule for its dysmotility pivotal clinical study.
More than 200 patients were recruited in a multi-site clinical trial to support a submission for initial U.S. regulatory clearance around the use of Atmo’s gas-sensing capsule to assess gastrointestinal motility disorders.
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