JOVS Electric Stimulation Beauty Device (JE2)
FDA 510(k) K250227 · Shenzhen Qianyu Technology Co., Ltd.
510(k) numberK250227
Submission
- Device name
- JOVS Electric Stimulation Beauty Device (JE2)
- Applicant
- Shenzhen Qianyu Technology Co., Ltd.
Shenzhen City, CN - Received
- January 27, 2025
- Decision date
- October 17, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K220645 | Hand-held IPL device (JOVS Hair Removal Device)OHT · Traditional | 04/27/2022SE |
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Questions and answers
When was JOVS Electric Stimulation Beauty Device (JE2) cleared by the FDA?
JOVS Electric Stimulation Beauty Device (JE2) (K250227) received a 510(k) decision of Substantially Equivalent on October 17, 2025, 263 days after the submission was received.
What is the product code of K250227?
The FDA product code is NFO – Stimulator, Transcutaneous Electrical, Aesthetic Purposes, a Class II (moderate risk) device regulated under 21 CFR 882.5890.