Hair Growth Laser Cap

FDA 510(k) K252325 · Cosmo Far East Technology Limited

Substantially Equivalent

510(k) numberK252325

Submission

Device name
Hair Growth Laser Cap
Applicant
Cosmo Far East Technology Limited
Shenzhen, CN
Received
July 25, 2025
Decision date
October 22, 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
OAP – Laser, Comb, Hair
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5500
Specialty
Physical Medicine

Promote hair growth in males with androgenic alopecia and norwood hamilton classification of iia to v

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K253349Hair Regrowth Cap (Model: T-119-HRC)OAP · Traditional Light Tree Ventures Europe B.V.12/24/2025SE
K252414Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1)OAP · Traditional Shenzhen Kaiyan Medical Equipment Co., Ltd.10/30/2025SE
K251017CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)OAP · Traditional Shenzhen Kaiyan Medical Equipment Co., Ltd.06/17/2025SE
K250467Red Light Hair Growth Cap (LP-RJVGRW-BLK)OAP · Traditional Shenzhen Idea Light Limited06/05/2025SE

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Questions and answers

When was Hair Growth Laser Cap cleared by the FDA?

Hair Growth Laser Cap (K252325) received a 510(k) decision of Substantially Equivalent on October 22, 2025, 89 days after the submission was received.

What is the product code of K252325?

The FDA product code is OAP – Laser, Comb, Hair, a Class II (moderate risk) device regulated under 21 CFR 890.5500.