510(k) K233473

Device
DEKA LOTUS
Applicant
El.En S.P.A.
510(k) number
K233473
Product code
ONF
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-16
Date received
2023-10-25
Regulation
878.4810
Classification name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Paolo Peruzzi
Address
Via Baldanzese 17 Calenzano IT 50041 50041

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code ONF#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K251545Intense Pulsed Light Therapy Device (MMABM-1)Micowey Medical Equipment (Guangxi) Co., Ltd.2025-09-04
K231952MEDILIGHTMedicreations, LLC2025-09-03
K243123IPL Treatment Device (MDSQMC-01)Medusa (Guangxi)Medical Devices Co., Ltd.2025-07-03
K250281DEKA LOTUSEl.En S.P.A.2025-02-26
K242440Intense Pulsed Light Treatment System (LK-PT)Nanjing Bestview Laser S&T Co., Ltd.2024-11-14
K240314MULA (K2-A1)Guangzhou Ciellulu Photoelectric Technology Co., Ltd.2024-08-21
K240482Intense Pulsed Light System (ST-690)Smedtrum Medical Technology Co., Ltd.2024-05-17
K233307Intensity Pulsed Light Therapy SystemBeijing Adss Development Co., Ltd.2024-03-15
K232708Intense pulsed light therapy deviceHebei Zhemai Technology Co., Ltd.2023-12-01
K232192Venus Versa PRO SystemVenus Concept, Inc.2023-09-11
K231394Intense Pulsed Light SystemSmedtrum Medical Technology Co., Ltd.2023-08-09
K230816Intense Pulsed Light Treatment SystemShangdong Huamei Technology Co., Ltd.2023-04-21
K220214Painless IPL System - KDT750Shanghai Omni Laser Skinology Co., Ltd.2023-02-18
K22079410PLTentech Co. , Ltd.2022-11-10
K221214Hand-held IPL device (IPL Home Use Hair Removal Device) Model:FZ-608, FZ-608G, FZ-100, FZ-200Shenzhen Ionka Medical Technology Co., Ltd.2022-09-21