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FDA 510(k)

CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)

K-Number: K251017 · 2025-06-17

ApplicantShenzhen Kaiyan Medical Equipment Co., Ltd.
Decision Date2025-06-17
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) is a medical device manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd.. It received FDA 510(k) clearance on 2025-06-17 under approval number K251017. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)?

CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) is a medical device that received FDA 510(k) clearance on 2025-06-17. It is manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd.. The 510(k) number is K251017.

When was CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) approved by the FDA?

CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) received FDA 510(k) clearance on 2025-06-17, under approval number K251017.

What company makes CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)?

CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) is manufactured by Shenzhen Kaiyan Medical Equipment Co., Ltd..

What is the FDA product code for CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A)?

The FDA product code for CurrentBody Skin Dual Light Hair Growth Helmet (model: MZ-07A) is OAP.

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Related PubMed Literature

PMID: 41779786 Stress-dependent growth in breast cancer arises from a mechano-osmotic coupling and cell-sizing checkpoint. Proceedings of the National Academy of Sciences of the United States of America (2026)

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Official Source

View on FDA Database →

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

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