Medical Device Manufacturer · IT , Calenzano

Elesta S.P.A - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
3
Total
3
Cleared
0
Denied

Elesta S.P.A has 3 FDA 510(k) cleared medical devices. Based in Calenzano, IT.

Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Elesta S.P.A Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Maurizio Pantaleoni and DuVal & Associates.

FDA 510(k) Regulatory Record - Elesta S.P.A
3 devices
1-3 of 3
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