FDA 510(k)

JOVS Electric Stimulation Beauty Device (JE2)

K-Number: K250227 · 2025-10-17

ApplicantShenzhen Qianyu Technology Co., Ltd.

Decision Date2025-10-17

Product CodeNFO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

JOVS Electric Stimulation Beauty Device (JE2) is a medical device manufactured by Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-10-17 under approval number K250227. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOVS Electric Stimulation Beauty Device (JE2)?

JOVS Electric Stimulation Beauty Device (JE2) is a medical device that received FDA 510(k) clearance on 2025-10-17. It is manufactured by Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K250227.

When was JOVS Electric Stimulation Beauty Device (JE2) approved by the FDA?

JOVS Electric Stimulation Beauty Device (JE2) received FDA 510(k) clearance on 2025-10-17, under approval number K250227.

What company makes JOVS Electric Stimulation Beauty Device (JE2)?

JOVS Electric Stimulation Beauty Device (JE2) is manufactured by Shenzhen Qianyu Technology Co., Ltd..

What is the FDA product code for JOVS Electric Stimulation Beauty Device (JE2)?

The FDA product code for JOVS Electric Stimulation Beauty Device (JE2) is NFO.

Related Clinical Trials

NCT05452226 Neuromuscular Electrical Stimulation in COPD/Community Acquired Pneumonia COMPLETED NCT06998134 Toward Ubiquitous Lower Limb Exoskeleton Use in Children and Young Adults RECRUITING NCT06868914 Phase I Trial of High-Density Theta Burst Stimulation (hdTBS) NOT_YET_RECRUITING NCT04935697 Non-invasive Vagal Neurostimulation (nVNS) for Traumatic Brain Injury (TBI)-Induced Acute Respiratory Distress COMPLETED NCT01961557 Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders COMPLETED NCT07099092 Causal Mechanisms of Odor-Guided Behavior in Humans NOT_YET_RECRUITING

Related PubMed Literature

PMID: 41475514 US FDA approves home-delivered tDCS for treating depression. Brain stimulation (2026) PMID: 35047938 Evolution of the Vagus Nerve Stimulation (VNS) Therapy System Technology for Drug-Resistant Epilepsy. Frontiers in medical technology (2021) PMID: 28331534 Ford and Edison in a modern regulatory environment: the first-in-human trial of night-work and artificial light. Journal of occupational medicine and toxicology (London, England) (2017)

Other Devices by Shenzhen Qianyu Technology Co., Ltd.

K220645Hand-held IPL device (JOVS Hair Removal Device) K214113Hand-held IPL device(JOVS Graphene Hair Removal Device) K231800IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 K240360Wrinkle Treatment Device (JM2) K244020Wrinkle Treatment Device (JM1, JM2B)

Related Devices (Code: NFO)

K152199RejuvatoneMDTrophy Skin, Inc. K150826Nutra Face Lift Model PE8050Nutra Luxe MD, LLC K163550Pobling MIITY 2Habalan Med & Beauty Co.,Ltd K162652Smart Photon Micro-current Device, Model: EP-300Li-Tek Electronic Technology Corporation K171647BeneLife Premium Facial Treatment Pack, Model: QZ0701AInfinitus (China) Company , Ltd. K171588NuBODY Skin Toning DeviceCarol Cole Company Dba Nuface

Official Source

View on FDA Database →

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