Memory MD, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Memory MD, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeuroCap (Model DEC22), NeuroCap, NeuroEEG
3
Total
3
Cleared
0
Denied
Memory MD, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2021. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Memory MD, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Guangzhou GLOMED Biological Technology Co., Ltd. and Mtak, LLC.
FDA 510(k) Regulatory Record - Memory MD, Inc.
3 devices