Zeto, Inc. - FDA 510(k) Cleared Devices
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 Medical Device Academy, Inc. and Innolitics, LLC.
3 devices