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FDA 510(k)

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

N.º K: K251825 · 2025-10-01

SolicitanteShenzhen Ulike Smart Electronics Co., Ltd.
Fecha de decisión2025-10-01
Código de productoOHS
Comité asesorSU
DecisiónSubstantially Equivalent

Resumen del dispositivo

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.

Preguntas frecuentes

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.

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Otros registros que enlistan a Shenzhen Ulike Smart Electronics Co., Ltd. como solicitante

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Dispositivos relacionados (Código: OHS)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

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Fuente oficial

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