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FDA 510(k)

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

K-Number: K260179 · 2026-06-03

ApplicantTouchbeauty Beauty & Health (Shenzhen) Co., Ltd.
Decision Date2026-06-03
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VITA Multi-Function Head Brush (TB-2343F, TB-2442F) is the device name listed in this FDA 510(k) record. The listed applicant is Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2026-06-03 under 510(k) number K260179. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA Multi-Function Head Brush (TB-2343F, TB-2442F)?

VITA Multi-Function Head Brush (TB-2343F, TB-2442F) is a medical device that received FDA 510(k) clearance on 2026-06-03. The listed applicant is Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. The 510(k) number is K260179.

When did VITA Multi-Function Head Brush (TB-2343F, TB-2442F) receive FDA 510(k) clearance?

VITA Multi-Function Head Brush (TB-2343F, TB-2442F) received FDA 510(k) clearance on 2026-06-03, under 510(k) number K260179.

Who is the listed applicant for VITA Multi-Function Head Brush (TB-2343F, TB-2442F)?

The FDA 510(k) record lists Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA Multi-Function Head Brush (TB-2343F, TB-2442F)?

The FDA product code for VITA Multi-Function Head Brush (TB-2343F, TB-2442F) is NFO.

Other records listing Touchbeauty Beauty & Health (Shenzhen) Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252053VITA Multi-Function Head Brush (TB-2443F, TB-2442AF, TB-2343F, TB-2442F)K251727GLAM LED Facial Mask (TB-2386F)K183217IPL Hair Removal Device

Related Devices (Code: NFO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253932FACEGYM Pro Device (HD-109)Shenzhen Kaiyan Medical Equipment Co., Ltd.K260895Ulike Clear Zero (YC10 BU)Guangxi Ulike Medical Technology Co., Ltd.K252621DeepSkin (DEP100)El Global Trade, Ltd.K252187Aura Glide (FC40)Aura Medical, LLCK252146Multi-functional Facial Beauty Device ( SKB-1703,SKB-1803,SKB-1909, SKB-2003 SKB-2109,SKB-2129,SKB-2208PRO, SKB-2209)Shenzhen Siken 3D Technology Development Co., Ltd.K250618Medi Lift Essential Eye MaskYa-Man, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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