Mahana Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mahana Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Mahana Parallel Digital Cognitive Behavioral Therapy (CBT) Mobile Application for Irritable Bowel Syndrome (IBS)
2
Total
1
Cleared
1
Denied
Mahana Therapeutics, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Last cleared in 2021. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mahana Therapeutics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mahana Therapeutics, Inc.
2 devices