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FDA 510(k)

LED Lip Perfector, model: ZC-05

K-Number: K223642 · 2023-03-09

ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-03-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LED Lip Perfector, model: ZC-05 is a medical device manufactured by Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-03-09 under approval number K223642. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED Lip Perfector, model: ZC-05?

LED Lip Perfector, model: ZC-05 is a medical device that received FDA 510(k) clearance on 2023-03-09. It is manufactured by Light Tree Ventures Europe B.V.. The 510(k) number is K223642.

When was LED Lip Perfector, model: ZC-05 approved by the FDA?

LED Lip Perfector, model: ZC-05 received FDA 510(k) clearance on 2023-03-09, under approval number K223642.

What company makes LED Lip Perfector, model: ZC-05?

LED Lip Perfector, model: ZC-05 is manufactured by Light Tree Ventures Europe B.V..

What is the FDA product code for LED Lip Perfector, model: ZC-05?

The FDA product code for LED Lip Perfector, model: ZC-05 is ILY.

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) K230720LUSTRE 3XPRESS Light Beauty Therapy patches, model: PR6001, PR5001 K223893Infrared Heat (Model: E0221)

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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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