ONG

Powered Laser Surgical Instrument With MicrobeamFractional Output

产品代码
ONG
器械名称
Powered Laser Surgical Instrument With MicrobeamFractional Output
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)
5 件
其中 Summary 已存档
4 份,可直接下载
FDA 历史累计 510(k)
35 件(全部年份;本站只收录近三年的明细)

FDA 分类定义

A LASER (Light Amplification by Stimulated Emission of Radiation) based device having coherence, collimated and typically monochromatic radiation. The laser output is in form of tiny beams in micro range. Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic to destroy, remove or coagulate tissue, generally soft tissue. 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, remove or coagulate 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)(5 件)

数据窗口为最近三年。最新一件:2025-10-20。

510(k) 号批准日期申请人器械名称摘要
K2521552025-10-20AVAVA, Inc.AVAVA™ Skin Treatment SystemPDF
K2440602025-07-31Lutronic CorporationeCO2 3DPDF
K2510312025-07-02Shanghai Apolo Medical Technology Co.,…Fiber Laser Treatment Systems (HS-232,HS-233)PDF
K2504022025-04-14AVAVA, Inc.AVAVA™ Skin Treatment SystemFDA
K2335502024-01-02Lutronic AestheticMOSAIC 3D (Surgical Laser)PDF

其中 4 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: ONG
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。