Magnus Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Magnus Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Magnus Neuromodulation System (MNS) with SAINT Technology, Model Number 1001K
1
Total
1
Cleared
0
Denied
Magnus Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Burlingame, US.
Last cleared in 2022. Active since 2022. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Magnus Medical, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Magnus Medical, Inc.
1 devices