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FDA 510(k)

LED Light Therapy Masks (LumiLips FAC07NA)

K-Number: K260202 · 2026-03-23

Decision Date2026-03-23
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LED Light Therapy Masks (LumiLips FAC07NA) is a medical device manufactured by Guangdong Newdermo Biotech Co., Ltd.. It received FDA 510(k) clearance on 2026-03-23 under approval number K260202. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED Light Therapy Masks (LumiLips FAC07NA)?

LED Light Therapy Masks (LumiLips FAC07NA) is a medical device that received FDA 510(k) clearance on 2026-03-23. It is manufactured by Guangdong Newdermo Biotech Co., Ltd.. The 510(k) number is K260202.

When was LED Light Therapy Masks (LumiLips FAC07NA) approved by the FDA?

LED Light Therapy Masks (LumiLips FAC07NA) received FDA 510(k) clearance on 2026-03-23, under approval number K260202.

What company makes LED Light Therapy Masks (LumiLips FAC07NA)?

LED Light Therapy Masks (LumiLips FAC07NA) is manufactured by Guangdong Newdermo Biotech Co., Ltd..

What is the FDA product code for LED Light Therapy Masks (LumiLips FAC07NA)?

The FDA product code for LED Light Therapy Masks (LumiLips FAC07NA) is OHS.

Related Clinical Trials

Related PubMed Literature

Other Devices by Guangdong Newdermo Biotech Co., Ltd.

Related Devices (Code: OHS)

Official Source

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