Arrive Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrive Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MI.BO. ® MyoBoost EMS System (MB-1000, MB-600, MB-400)
1
Total
1
Cleared
0
Denied
Arrive Systems, Inc. has 1 FDA 510(k) cleared medical devices. Based in New Ark, US.
Last cleared in 2021. Active since 2021. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Arrive Systems, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Iuvo Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Arrive Systems, Inc.
1 devices