Nu Skin RenuSpa iO
K-Number: K232001 · 2023-11-21
Device Summary
Frequently Asked Questions
What is the Nu Skin RenuSpa iO?
Nu Skin RenuSpa iO is a medical device that received FDA 510(k) clearance on 2023-11-21. The listed applicant is Nse Products, Inc.. The 510(k) number is K232001.
When did Nu Skin RenuSpa iO receive FDA 510(k) clearance?
Nu Skin RenuSpa iO received FDA 510(k) clearance on 2023-11-21, under 510(k) number K232001.
Who is the listed applicant for Nu Skin RenuSpa iO?
The FDA 510(k) record lists Nse Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nu Skin RenuSpa iO?
The FDA product code for Nu Skin RenuSpa iO is NFO.
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.