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FDA 510(k)

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001

K-Number: K230720 · 2023-07-03

ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-07-03
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is a medical device manufactured by Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-07-03 under approval number K230720. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is a medical device that received FDA 510(k) clearance on 2023-07-03. It is manufactured by Light Tree Ventures Europe B.V.. The 510(k) number is K230720.

When was LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 approved by the FDA?

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 received FDA 510(k) clearance on 2023-07-03, under approval number K230720.

What company makes LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is manufactured by Light Tree Ventures Europe B.V..

What is the FDA product code for LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001?

The FDA product code for LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 is OLP.

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Related PubMed Literature

PMID: 40417352 Regulatory aspects of optogenetic research and therapy for retinitis pigmentosa under EU law. Frontiers in medical technology (2025)

Other Devices by Light Tree Ventures Europe B.V.

K221775LED Light Therapy Mask (model: MK-78, MK-04, MK66-H, MK66R-B, EL00003) K221444LED Eye Perfector, model: EY-36A, EY-36B K221946LED Light Therapy Mask (model: MK66R-B) K222205Cold Sore Device (Model: QPZ-01) K223893Infrared Heat (Model: E0221) K230597Aduro Comb (Model: SZ-22, SZ-22A, SZ-22B)

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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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