Leadoptik, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Leadoptik, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIA-1 Catheter (542-1), LIA Console (542-7)
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: General & Plastic Surgery.
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.
FDA 510(k) Regulatory Record - Leadoptik, Inc.
2 devices