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FDA PRODUCT CODE · CLASS II

ONFPowered Light Based Non-Laser Surgical Instrument With Thermal Effect

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.

DEVICE CLASS
Class II
REGULATION
21 CFR 878.4810
MEDICAL SPECIALTY
General, Plastic Surgery
REVIEW PANEL
SU
ImplantLife-sustainingGMP-exemptThird-party review eligible
6
510(K)/PMA CLEARANCES
510k: 6
0
RECALL ENTRIES

Recent clearances

K261204Sanhe LEFIS Electronics Co., Ltd. · 510k2026-06-12
K251545Micowey Medical Equipment (Guangxi) Co., Ltd. · 510k2025-09-04
K231952Medicreations, LLC · 510k2025-09-03
K243123Medusa (Guangxi)Medical Devices Co., Ltd. · 510k2025-07-03
K250281El.En S.P.A. · 510k2025-02-26
K242440Nanjing Bestview Laser S&T Co., Ltd. · 510k2024-11-14

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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