Medical Device Manufacturer · ES , Gij?n

Leaseir Technologies, Slu - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Leaseir Technologies, Slu has 1 FDA 510(k) cleared medical devices. Based in Gij?n, ES.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Leaseir Technologies, Slu

1 devices

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