FDA 510(k)

LipoSurg ARTIST

K-Number: K254135 · 2026-09-05

Decision Date2026-09-05

Product CodeQPB

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LipoSurg ARTIST is the device name listed in this FDA 510(k) record. The listed applicant is NOUVAG AG. It received FDA 510(k) clearance on 2026-09-05 under 510(k) number K254135. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LipoSurg ARTIST?

LipoSurg ARTIST is a medical device that received FDA 510(k) clearance on 2026-09-05. The listed applicant is NOUVAG AG. The 510(k) number is K254135.

When did LipoSurg ARTIST receive FDA 510(k) clearance?

LipoSurg ARTIST received FDA 510(k) clearance on 2026-09-05, under 510(k) number K254135.

Who is the listed applicant for LipoSurg ARTIST?

The FDA 510(k) record lists NOUVAG AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LipoSurg ARTIST?

The FDA product code for LipoSurg ARTIST is QPB.

Related Devices (Code: QPB)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.