Magnolia Medical Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Magnolia Medical Technologies - FDA 510(k) Cleared Devices
Recent clearances: Steripath® Flow™ Blood Collection System, Steripath Micro Blood Collection System
2
Total
2
Cleared
0
Denied
Magnolia Medical Technologies has 2 FDA 510(k) cleared medical devices. Based in Seattle, US.
Latest FDA clearance: Sep 2025. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Magnolia Medical Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Magnolia Medical Technologies
2 devices