Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)
K-Number: K251034 · 2025-10-12
Device Summary
Frequently Asked Questions
What is the Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) is a medical device that received FDA 510(k) clearance on 2025-10-12. It is manufactured by Shenzhen Nuon Medical Equipment Co., Ltd.. The 510(k) number is K251034.
When was Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) approved by the FDA?
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) received FDA 510(k) clearance on 2025-10-12, under approval number K251034.
What company makes Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?
Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) is manufactured by Shenzhen Nuon Medical Equipment Co., Ltd..
What is the FDA product code for Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44)?
The FDA product code for Radiant Renewal Skincare Lid (HD-59A, HD-59B, HD-70); Radiant Renewal Skincare Wand (HD-44) is NFO.
Other Devices by Shenzhen Nuon Medical Equipment Co., Ltd.
Related Devices (Code: NFO)
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.