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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 the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. It received FDA 510(k) clearance on 2025-10-01 under 510(k) 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. The listed applicant is Shenzhen Ulike Smart Electronics Co., Ltd.. The 510(k) number is K251825.

When did Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG) receive FDA 510(k) clearance?

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

Who is the listed applicant for Jmoon FlexGlow Light Therapy Device (JD20U SP, JD20U SG)?

The FDA 510(k) record lists Shenzhen Ulike Smart Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Shenzhen Ulike Smart Electronics Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 23 devices →

Related Devices (Code: OHS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.