Eneura, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eneura, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SAVI Dual (TM) Migraine Therapy, SpringTMS
4
Total
4
Cleared
0
Denied
Eneura, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Last cleared in 2023. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Eneura, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Larry W. Getlin as regulatory consultant.
FDA 510(k) Regulatory Record - Eneura, Inc.
4 devices