ONF

Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

产品代码
ONF
器械名称
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
管理类别
第 2 类(Class II)
21 CFR 条款
21 CFR 878.4810
FDA 专业组
General, Plastic Surgery
上市路径
需提交 510(k) 上市前通告
标记
可走第三方审查
该代码近三年的 510(k)
12 件
其中 Summary 已存档
8 份,可直接下载
FDA 历史累计 510(k)
74 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

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.

定义原文来自 FDA 器械分类库,属美国联邦政府作品(公有领域)。

该代码近三年的 510(k)(12 件)

数据窗口为最近三年。最新一件:2026-06-12。

510(k) 号批准日期申请人器械名称摘要
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

其中 8 件的 Summary 已存档在本站,点 PDF 直接下载;其余给 FDA 官方链接。

FDA 官方分类页: ONF
分类与上市路径以 FDA 现行公告为准。本页数据来自 openFDA(CC0 公有领域),不构成注册策略建议。