Nuna Lux (NUNL528)

FDA 510(k) K233862 · Premier North America, Inc.

Substantially Equivalent

510(k) numberK233862

Submission

Device name
Nuna Lux (NUNL528)
Applicant
Premier North America, Inc.
Fort Lauderdale, FL, US
Received
December 6, 2023
Decision date
March 1, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OHS – Light Based Over The Counter Wrinkle Reduction
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

Use of light based treatment to reduce wrinkles on the body in general or specific anatomical locations depending on the information provided.

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K261851LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED…OHS · Traditional Shenzhen Qianyu Technology Co., Ltd.08/04/2026SE
K261496LED Light Therapy Masks (PE748, PE749, PE756)OHS · Traditional Duplex International Trading Limited08/04/2026SE
K261482LightStim for Wrinkles (1984); LightStim for Acne (2038)OHS · Traditional Led Intellectual Properties, LLC07/31/2026SE
K2605985 Wavelength LED Facemask (TN2508)OHS · Traditional iSMART Developments, Ltd.07/24/2026SE
K261407XPREEN LED Light Therapy Masks (XPRE322, XPRE326, XPRE327, XPRE342, XPRE368, XPRE422…OHS · Traditional Dongguan Miqiang Technology Co., Ltd.07/15/2026SE
K261473ChromixOHS · Traditional Termosalud S.L.07/01/2026SE
K261052LED Light Therapy Masks (LED Face Mask Pro FAC08NA, LED Chest Mask Pro FAC09NA)OHS · Traditional Guangdong Newdermo Biotech Co., Ltd.06/29/2026SE

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Questions and answers

When was Nuna Lux (NUNL528) cleared by the FDA?

Nuna Lux (NUNL528) (K233862) received a 510(k) decision of Substantially Equivalent on March 1, 2024, 86 days after the submission was received.

What is the product code of K233862?

The FDA product code is OHS – Light Based Over The Counter Wrinkle Reduction, a Class II (moderate risk) device regulated under 21 CFR 878.4810.