Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)— 510(k) K251034

Name: FDA 510(k) clearance K251034
Creator: U.S. Food and Drug Administration
Published: 2025-10-12

Substantially Equivalent

Shenzhen Nuon Medical Equipment Co., Ltd.

FDA 510(k) clearance K251034 for Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44), Substantially Equivalent on 2025-10-12. Applicant: Shenzhen Nuon Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Nuon Medical Equipment Co., Ltd.
Product code: Code NFO
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2025-04-03
Decision date: 2025-10-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

Download summary PDF View on FDA.gov ↗

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