El.En Electronic Engineering Spa
El.En Electronic Engineering Spa holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2023.
Top product codes for El.En Electronic Engineering Spa
Recent clearances by El.En Electronic Engineering Spa
- K222221 — DEKA HELIX
- K213658 — DEKA SMARTPERIO
- K212270 — DEKA LipoAI
- K211091 — Deka Tiac II
- K211362 — SCAR 3
- K203396 — DEKA SMARTPERIO
- K211821 — DEKA Motus AZ
- K202258 — ERISE Laser handpiece
- K202079 — Physiq
- K192539 — Deka Luxea
- K181867 — Deka Smartxide2 Trio
- K181510 — ECHOLASER X4
- K181486 — DEKA Motus AY
- K180193 — DEKA SMARTXIDE Family (Smartxide Touch, Smartxide Punto)
- K172362 — DEKA SMARTXIDE TOUCH
- K172363 — DEKA SMARTXIDE ULTRASPEED
- K162886 — DEKA MOTUS AX
- K150516 — DEKA SYNCHRO REPLA:Y FAMILY OF LASER SYSTEMS
- K131095 — DEKA SYNCHRO REPLA: Y FAMILY OF LASER SYSTEMS
- K113504 — DEKA SMARTXIDE AND DELIVERY ACCESSORIES
- K122125 — ASA LASER SH1
- K103288 — DEKA SYNCHRO FT
- K101904 — SMARTXIDE 50 HS/MS
- K082040 — MINISILK FT
- K082039 — SYNCHRO HP PLATFORM
- K072159 — SMART CO2 (SMARTXIDE, SMART US20D) WITH DOT SCANNER
- K062762 — DERMA YAG
Data sourced from openFDA. This site is unofficial and independent of the FDA.