Duopross Meditech Corporate - FDA 510(k) Cleared Devices

Duopross Meditech Corporate has 1 FDA 510(k) cleared medical devices. Based in Farmingdale, US.

Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Duopross Meditech Corporate Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Shanghai SUNGO Management Consulting Co., Ltd. as regulatory consultant.