Duopross Meditech Corporate - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
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.
FDA 510(k) cleared devices by Duopross Meditech Corporate
1 devices