HIGHERDOSE Red Light Hat (HG-120K)

FDA 510(k) K242363 · Shenzhen Kaiyan Medical Equipment Co., Ltd.

Substantially Equivalent

510(k) numberK242363

Submission

Device name
HIGHERDOSE Red Light Hat (HG-120K)
Applicant
Shenzhen Kaiyan Medical Equipment Co., Ltd.
Shenzhen, CN
Received
August 9, 2024
Decision date
November 20, 2024
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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K252414Q-Renew LLLT Hair Growth Helmet (Q-HLMT-V1)OAP · Traditional Shenzhen Kaiyan Medical Equipment Co., Ltd.10/30/2025SE
K252325Hair Growth Laser CapOAP · Traditional Cosmo Far East Technology Limited10/22/2025SE
K251017CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)OAP · Traditional Shenzhen Kaiyan Medical Equipment Co., Ltd.06/17/2025SE

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Questions and answers

When was HIGHERDOSE Red Light Hat (HG-120K) cleared by the FDA?

HIGHERDOSE Red Light Hat (HG-120K) (K242363) received a 510(k) decision of Substantially Equivalent on November 20, 2024, 103 days after the submission was received.

What is the product code of K242363?

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