El.En S.P.A.

FDA Regulatory Profile

El.En S.P.A. appears in FDA public data with 0 recalls, 15 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 2, 2026.

Summary

Total Recalls
0
510(k) Clearances
15
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260647SPECCHIOApril 2, 2026
K251432OloAugust 6, 2025
K243683Deka BluebeamJune 12, 2025
K250281DEKA LOTUSFebruary 26, 2025
K241459MOTUS PRO FamilyJune 21, 2024
K240752DEKA TOROMay 16, 2024
K233473DEKA LOTUSMay 16, 2024
K234057NIRVANAApril 10, 2024
K240537SMARTXIDE PROMarch 20, 2024
K240497Smartxide Tetra ProMarch 12, 2024
K233470DEKA LILYDecember 19, 2023
K233090DEKA AGAIN PRO familyOctober 27, 2023
K231971DEKA PHYSIQ 360September 26, 2023
K232334DEKA SIMONSeptember 1, 2023
K133895DEKA SMARTXIDE LASER SYSTEMSeptember 5, 2014