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FDA 510(k)

GLAM LED Facial Mask (TB-2386F)

K-Number: K251727 · 2025-08-29

Decision Date2025-08-29
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GLAM LED Facial Mask (TB-2386F) is a medical device manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2025-08-29 under approval number K251727. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLAM LED Facial Mask (TB-2386F)?

GLAM LED Facial Mask (TB-2386F) is a medical device that received FDA 510(k) clearance on 2025-08-29. It is manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. The 510(k) number is K251727.

When was GLAM LED Facial Mask (TB-2386F) approved by the FDA?

GLAM LED Facial Mask (TB-2386F) received FDA 510(k) clearance on 2025-08-29, under approval number K251727.

What company makes GLAM LED Facial Mask (TB-2386F)?

GLAM LED Facial Mask (TB-2386F) is manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd..

What is the FDA product code for GLAM LED Facial Mask (TB-2386F)?

The FDA product code for GLAM LED Facial Mask (TB-2386F) is GEX. This falls under the Gastroenterology category.

Other Devices by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

Related Devices (Code: GEX)

Official Source

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