GLAM LED Facial Mask (TB-2386F)

FDA 510(k) K251727 · Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

Substantially Equivalent

510(k) numberK251727

Submission

Device name
GLAM LED Facial Mask (TB-2386F)
Applicant
Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.
Shenzhen, CN
Received
June 5, 2025
Decision date
August 29, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GEX – Powered Laser Surgical Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue, for general surgical purpose in medical specialties of general and plastic surgery, dermatology/aesthetic, podiatry, otolaryngology (ent), gynecology…

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Questions and answers

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

GLAM LED Facial Mask (TB-2386F) (K251727) received a 510(k) decision of Substantially Equivalent on August 29, 2025, 85 days after the submission was received.

What is the product code of K251727?

The FDA product code is GEX – Powered Laser Surgical Instrument, a Class II (moderate risk) device regulated under 21 CFR 878.4810.