JOVS Electric Stimulation Beauty Device (JE2)
K-Number: K250227 · 2025-10-17
Device Summary
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. The listed applicant is Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K250227.
When did JOVS Electric Stimulation Beauty Device (JE2) receive FDA 510(k) clearance?
JOVS Electric Stimulation Beauty Device (JE2) received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250227.
Who is the listed applicant for JOVS Electric Stimulation Beauty Device (JE2)?
The FDA 510(k) record lists Shenzhen Qianyu Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Shenzhen Qianyu Technology 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.
Related Devices (Code: NFO)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.