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

Tentech, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Bt Solutions, Inc. as regulatory consultant.