Sentienx Sdn Bhd - FDA 510(k) Cleared Devices

Sentienx Sdn Bhd has 1 FDA 510(k) cleared medical devices. Based in Kulim, MY.

Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Sentienx Sdn Bhd Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Tg Medical USA (Inc) as regulatory consultant.