Leadoptik, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Leadoptik, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Leadoptik, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Qserve Group and Qserve Group US.
2 devices