ONF
- 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.
510(k) clearances, last 3 years (12)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K261204 | 2026-06-12 | Sanhe LEFIS Electronics Co., Ltd. | Intense Pulsed Light Therapy Device | |
| K251545 | 2025-09-04 | Micowey Medical Equipment (Guangxi) Co… | Intense Pulsed Light Therapy Device (MMABM-1) | |
| K231952 | 2025-09-03 | Medicreations, LLC | MEDILIGHT | — |
| K243123 | 2025-07-03 | Medusa (Guangxi)Medical Devices Co., L… | IPL Treatment Device (MDSQMC-01) | |
| K250281 | 2025-02-26 | El.En S.P.A. | DEKA LOTUS | |
| K242440 | 2024-11-14 | Nanjing Bestview Laser S&T Co., Ltd. | Intense Pulsed Light Treatment System (LK-PT) | |
| K240314 | 2024-08-21 | Guangzhou Ciellulu Photoelectric Techn… | MULA (K2-A1) | FDA |
| K240482 | 2024-05-17 | Smedtrum Medical Technology Co., Ltd. | Intense Pulsed Light System (ST-690) | |
| K233473 | 2024-05-16 | El.En S.P.A. | DEKA LOTUS | |
| K233307 | 2024-03-15 | Beijing Adss Development Co., Ltd. | Intensity Pulsed Light Therapy System | — |
| K232708 | 2023-12-01 | Hebei Zhemai Technology Co., Ltd. | Intense pulsed light therapy device | |
| K232192 | 2023-09-11 | Venus Concept, Inc. | Venus Versa PRO System | FDA |
Official FDA classification page: ONF
Classification and pathway per current FDA publications. Data from openFDA (CC0).