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FDA 510(k)

MEDILIGHT

K-Number: K231952 · 2025-09-03

ApplicantMedicreations, LLC
Decision Date2025-09-03
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDILIGHT is a medical device manufactured by Medicreations, LLC. It received FDA 510(k) clearance on 2025-09-03 under approval number K231952. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDILIGHT?

MEDILIGHT is a medical device that received FDA 510(k) clearance on 2025-09-03. It is manufactured by Medicreations, LLC. The 510(k) number is K231952.

When was MEDILIGHT approved by the FDA?

MEDILIGHT received FDA 510(k) clearance on 2025-09-03, under approval number K231952.

What company makes MEDILIGHT?

MEDILIGHT is manufactured by Medicreations, LLC.

What is the FDA product code for MEDILIGHT?

The FDA product code for MEDILIGHT is ONF.

Other Devices by Medicreations, LLC

K231948MEDIYAG K231950MEDIDIODE

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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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