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FDA 510(k)

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)

K-Number: K251825 · 2025-10-01

Decision Date2025-10-01
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is a medical device manufactured by Shenzhen Ulike Smart Electronics Co., Ltd.. It received FDA 510(k) clearance on 2025-10-01 under approval number K251825. 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 Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is a medical device that received FDA 510(k) clearance on 2025-10-01. It is manufactured by Shenzhen Ulike Smart Electronics Co., Ltd.. The 510(k) number is K251825.

When was Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) approved by the FDA?

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) received FDA 510(k) clearance on 2025-10-01, under approval number K251825.

What company makes Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?

Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is manufactured by Shenzhen Ulike Smart Electronics Co., Ltd..

What is the FDA product code for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?

The FDA product code for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) is OHS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.