VITA Multi-Function Head Brush (TB-2343F, TB-2442F)

Q: What is the product code of K260179?

The FDA product code is NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes, a Class II (moderate risk) device regulated under 21 CFR 882.5890.

FDA 510(k) K260179 · Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

Substantially Equivalent

510(k) numberK260179

Submission

Device name: VITA Multi-Function Head Brush (TB-2343F, TB-2442F)
Applicant: Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.
Shenzhen, CN
Received: January 21, 2026
Decision date: June 3, 2026
Decision: Substantially Equivalent (SESE)
Type: Traditional 510(k)
Summary: 510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code: NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Device class: Class II (moderate risk)
Regulation: 21 CFR 882.5890
Specialty: Neurology

Other 510(k)s with product code NFO

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K253932	FACEGYM Pro Device (HD-109)NFO · Traditional	Shenzhen Kaiyan Medical Equipment Co., Ltd.	07/23/2026SE
K260895	Ulike Clear Zero (YC10 BU)NFO · Traditional	Guangxi Ulike Medical Technology Co., Ltd.	05/28/2026SE
K252621	DeepSkin (DEP100)NFO · Traditional	El Global Trade, Ltd.	05/08/2026SE
K252187	Aura Glide (FC40)NFO · Traditional	Aura Medical, LLC	12/23/2025SE
K252146	Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003…NFO · Traditional	Shenzhen Siken 3D Technology Development Co., Ltd.	12/23/2025SE
K250618	Medi Lift Essential Eye MaskNFO · Traditional	Ya-Man, Ltd.	10/29/2025SE
K250227	JOVS Electric Stimulation Beauty Device (JE2)NFO · Traditional	Shenzhen Qianyu Technology Co., Ltd.	10/17/2025SE
K251034	Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand…NFO · Traditional	Shenzhen Nuon Medical Equipment Co., Ltd.	10/12/2025SE

More from Shenzhen Nuon Medical Equipment Co., Ltd.

510(k)	Device	Decision
K252053	VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F)OHS · Traditional	10/27/2025SE
K251727	GLAM LED Facial Mask (TB-2386F)GEX · Traditional	08/29/2025SE
K183217	IPL Hair Removal DeviceOHT · Traditional	02/15/2019SE

Questions and answers

When was VITA Multi-Function Head Brush (TB-2343F, TB-2442F) cleared by the FDA?

VITA Multi-Function Head Brush (TB-2343F, TB-2442F) (K260179) received a 510(k) decision of Substantially Equivalent on June 3, 2026, 133 days after the submission was received.

What is the product code of K260179?

The FDA product code is NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes, a Class II (moderate risk) device regulated under 21 CFR 882.5890.