El.En Electronic Engineering Spa

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K222221DEKA HELIXJanuary 4, 2023
K213658DEKA SMARTPERIOMarch 11, 2022
K212270DEKA LipoAIOctober 21, 2021
K211091Deka Tiac IIOctober 15, 2021
K211362SCAR 3August 25, 2021
K203396DEKA SMARTPERIOAugust 23, 2021
K211821DEKA Motus AZJuly 6, 2021
K202258ERISE Laser handpieceApril 26, 2021
K202079PhysiqNovember 25, 2020
K192539Deka LuxeaDecember 16, 2019
K181867Deka Smartxide2 TrioOctober 2, 2018
K181510ECHOLASER X4September 4, 2018
K181486DEKA Motus AYAugust 30, 2018
K180193DEKA SMARTXIDE Family (Smartxide Touch, Smartxide Punto)February 21, 2018
K172363DEKA SMARTXIDE ULTRASPEEDNovember 17, 2017
K172362DEKA SMARTXIDE TOUCHNovember 17, 2017
K162886DEKA MOTUS AXJune 19, 2017
K150516DEKA SYNCHRO REPLA:Y FAMILY OF LASER SYSTEMSApril 13, 2015
K131095DEKA SYNCHRO REPLA: Y FAMILY OF LASER SYSTEMSDecember 5, 2013
K113504DEKA SMARTXIDE AND DELIVERY ACCESSORIESFebruary 1, 2013