Oncopatch, Inc. - FDA 510(k) Cleared Devices

Oncopatch, Inc. has 1 FDA 510(k) cleared medical devices. Based in Aurora, US.

Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Oncopatch, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by TAMM Net, Inc. as regulatory consultant.