Medeia, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medeia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BrainView QEEG Software, NeuralScan System, VitalScan ANS
4
Total
4
Cleared
0
Denied
Medeia, Inc. has 4 FDA 510(k) cleared medical devices. Based in Miami, US.
Last cleared in 2023. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medeia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance and Regulatory Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medeia, Inc.
4 devices