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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 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 2025-08-29 under 510(k) 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. The listed applicant is Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. The 510(k) number is K251727.

When did GLAM LED Facial Mask (TB-2386F) receive FDA 510(k) clearance?

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

Who is the listed applicant for GLAM LED Facial Mask (TB-2386F)?

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 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.

Related Clinical Trials

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.

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.

Related Devices (Code: GEX)

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.

Official Source

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