Magnolia Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Magnolia Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Steripath Micro Blood Collection System, Steripath Gen2 Blood Collection System
2
Total
2
Cleared
0
Denied
Magnolia Medical Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Seattle, US.
Historical record: 2 cleared submissions from 2020 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Magnolia Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Magnolia Medical Technologies, Inc.
2 devices