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FDA 510(k)

SOLIUS PRO UVB Light Panel

K-Number: K252960 · 2026-01-16

ApplicantSolius Labs, Inc.
Decision Date2026-01-16
Product CodeSGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SOLIUS PRO UVB Light Panel is a medical device manufactured by Solius Labs, Inc.. It received FDA 510(k) clearance on 2026-01-16 under approval number K252960. The device is classified under product code SGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLIUS PRO UVB Light Panel?

SOLIUS PRO UVB Light Panel is a medical device that received FDA 510(k) clearance on 2026-01-16. It is manufactured by Solius Labs, Inc.. The 510(k) number is K252960.

When was SOLIUS PRO UVB Light Panel approved by the FDA?

SOLIUS PRO UVB Light Panel received FDA 510(k) clearance on 2026-01-16, under approval number K252960.

What company makes SOLIUS PRO UVB Light Panel?

SOLIUS PRO UVB Light Panel is manufactured by Solius Labs, Inc..

What is the FDA product code for SOLIUS PRO UVB Light Panel?

The FDA product code for SOLIUS PRO UVB Light Panel is SGZ.

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.

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