El.En S.P.A. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
El.En S.P.A. has 14 FDA 510(k) cleared general & plastic surgery devices. Based in Hopkinton, US.
Latest FDA clearance: Aug 2025. Active since 2014.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by El.En S.P.A.
14 devices
Cleared
Aug 06, 2025
Olo
General & Plastic Surgery
90d
Cleared
Jun 12, 2025
Deka Bluebeam
General & Plastic Surgery
195d
Cleared
Feb 26, 2025
DEKA LOTUS
General & Plastic Surgery
26d
Cleared
Jun 21, 2024
MOTUS PRO Family
General & Plastic Surgery
29d
Cleared
May 16, 2024
DEKA LOTUS
General & Plastic Surgery
204d
Cleared
May 16, 2024
DEKA TORO
General & Plastic Surgery
58d
Cleared
Apr 10, 2024
NIRVANA
General & Plastic Surgery
110d
Cleared
Mar 20, 2024
SMARTXIDE PRO
General & Plastic Surgery
23d
Cleared
Mar 12, 2024
Smartxide Tetra Pro
General & Plastic Surgery
21d
Cleared
Dec 19, 2023
DEKA LILY
Physical Medicine
55d
Cleared
Oct 27, 2023
DEKA AGAIN PRO family
General & Plastic Surgery
31d
Cleared
Sep 26, 2023
DEKA PHYSIQ 360
General & Plastic Surgery
85d