Nova HD+
K-Number: K262788 · 2026-08-31
Device Summary
Frequently Asked Questions
What is the Nova HD+?
Nova HD+ is a medical device that received FDA 510(k) clearance on 2026-08-31. The listed applicant is Aura Wellness, LLC. The 510(k) number is K262788.
When did Nova HD+ receive FDA 510(k) clearance?
Nova HD+ received FDA 510(k) clearance on 2026-08-31, under 510(k) number K262788.
Who is the listed applicant for Nova HD+?
The FDA 510(k) record lists Aura Wellness, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Nova HD+?
The FDA product code for Nova HD+ is SGT.
Other records listing Aura Wellness, LLC 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: SGT)
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.