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FDA 510(k)

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)

K-Number: K230336 · 2023-04-05

ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-04-05
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is the device name listed in this FDA 510(k) record. The listed applicant is Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-04-05 under 510(k) number K230336. 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™ Led Hair Regrowth(Model: MZ-07)?

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is a medical device that received FDA 510(k) clearance on 2023-04-05. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K230336.

When did CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) receive FDA 510(k) clearance?

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) received FDA 510(k) clearance on 2023-04-05, under 510(k) number K230336.

Who is the listed applicant for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

The FDA 510(k) record lists Light Tree Ventures Europe B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

The FDA product code for CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is OAP.

Other records listing Light Tree Ventures Europe B.V. as applicant

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Related Devices (Code: OAP)

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.

K261675CHZL Red Light Therapy Hair Growth Cap (Model(s):CHZL-120BK-L52D,CHZL-120BK-L53D,CHZL-120BK-L54D)Shenzhen Chuanghong Zhilian Technology Co., Ltd.K261253Laser Hair Growth Devices (HR-H1, HR-H2, HR-H3, HR-H4, HR-H5, HR-H6, HR-H7, HR-H8, HR-H9, HR-H10, HR-I1, HR-I2, HR-I3, HR-I4, HR-I5)Ziree Co., Ltd.K260899Laser Hair Growth Device (F21151, F21152, F21153, F21154, F21155, F21156, F21157, F21158, F21159)Zdeer Technology (Henan) Co., Ltd.K253231Laser Hair Growth System (Laser Cap 128, Laser Helmet 272, Laser Helmet 352, Laser Helmet 552, Laser Helmet 500)Hubei Yjt Technology Co.,LtdK251684Alma TED+ SystemAlma Lasers, Inc.K253669TRUDERMAL HALO HAIR GROWTH SYSTEM (M-180A); ADURO HAIR GROWTH (M-130,M-300)Shenzhen Kaiyan Medical Equipment Co., Ltd.

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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