Wrinkle Treatment Device (JM1, JM2B)

FDA 510(k) K244020 · Shenzhen Qianyu Technology Co., Ltd.

Substantially Equivalent

510(k) numberK244020

Submission

Device name
Wrinkle Treatment Device (JM1, JM2B)
Applicant
Shenzhen Qianyu Technology Co., Ltd.
Shenzhen, CN
Received
December 27, 2024
Decision date
May 1, 2025
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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K261482LightStim for Wrinkles (1984); LightStim for Acne (2038)OHS · Traditional Led Intellectual Properties, LLC07/31/2026SE
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More from Guangdong Newdermo Biotech Co., Ltd.

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K261851LED Light Therapy Mask (JML1, JML1+JML2); LED Light Therapy Mask (JML3, JML3+JML4); LED…OHS · Traditional 08/04/2026SE
K250227JOVS Electric Stimulation Beauty Device (JE2)NFO · Traditional 10/17/2025SE
K240360Wrinkle Treatment Device (JM2)OHS · Traditional 04/05/2024SE
K231800IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9OHT · Traditional 09/07/2023SE
K220645Hand-held IPL device (JOVS Hair Removal Device)OHT · Traditional 04/27/2022SE
K214113Hand-held IPL device(JOVS Graphene Hair Removal Device)OHT · Traditional 03/28/2022SE

Questions and answers

When was Wrinkle Treatment Device (JM1, JM2B) cleared by the FDA?

Wrinkle Treatment Device (JM1, JM2B) (K244020) received a 510(k) decision of Substantially Equivalent on May 1, 2025, 125 days after the submission was received.

What is the product code of K244020?

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.