ONF

Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Product code
ONF
Device name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Device class
Class 2
21 CFR
21 CFR 878.4810
Medical specialty
General, Plastic Surgery
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (last 3 years)
12
Summaries archived here
8 (direct download)
510(k) clearances (all years, FDA)
74 (all years; only the last 3 years are listed here)

FDA classification definition

A light based non-laser device that provides thermal effect including broad spectrum source devices such as intense pulse light (ipl). Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic. Indication for use can be general and/or specific.The classification regulation 21 cfr 878.4810 describes a device that is carbon dioxide or argon laser intended to cut, destroy, or remove tissue by the light.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (12)

Last three years. Most recent: 2026-06-12.

NumberDecision dateApplicantDevice nameSummary
K2612042026-06-12Sanhe LEFIS Electronics Co., Ltd.Intense Pulsed Light Therapy DevicePDF
K2515452025-09-04Micowey Medical Equipment (Guangxi) Co…Intense Pulsed Light Therapy Device (MMABM-1)PDF
K2319522025-09-03Medicreations, LLCMEDILIGHT
K2431232025-07-03Medusa (Guangxi)Medical Devices Co., L…IPL Treatment Device (MDSQMC-01)PDF
K2502812025-02-26El.En S.P.A.DEKA LOTUSPDF
K2424402024-11-14Nanjing Bestview Laser S&T Co., Ltd.Intense Pulsed Light Treatment System (LK-PT)PDF
K2403142024-08-21Guangzhou Ciellulu Photoelectric Techn…MULA (K2-A1)FDA
K2404822024-05-17Smedtrum Medical Technology Co., Ltd.Intense Pulsed Light System (ST-690)PDF
K2334732024-05-16El.En S.P.A.DEKA LOTUSPDF
K2333072024-03-15Beijing Adss Development Co., Ltd.Intensity Pulsed Light Therapy System
K2327082023-12-01Hebei Zhemai Technology Co., Ltd.Intense pulsed light therapy devicePDF
K2321922023-09-11Venus Concept, Inc.Venus Versa PRO SystemFDA

8 summaries are archived here for direct download.

Official FDA classification page: ONF
Classification and pathway per current FDA publications. Data from openFDA (CC0).