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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 a medical device manufactured by Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-04-05 under approval 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. It is manufactured by Light Tree Ventures Europe B.V.. The 510(k) number is K230336.

When was CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) approved by the FDA?

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

What company makes CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07)?

CurrentBody Skin™ Led Hair Regrowth(Model: MZ-07) is manufactured by Light Tree Ventures Europe B.V..

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 Devices by Light Tree Ventures Europe B.V.

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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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