Zeto, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Zeto, Inc. - FDA 510(k) Cleared Devices
Recent clearances: New Wave System, Flexset System, WR19 System
3
Total
3
Cleared
0
Denied
Zeto, Inc. has 3 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Latest FDA clearance: Mar 2026. Active since 2018. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Zeto, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biologics Consulting Group, Medical Device Academy, Inc. and Innolitics, LLC.
FDA 510(k) Regulatory Record - Zeto, Inc.
3 devices