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FDA 510(k)

Inbentus Versatile

K-Number: K252663 · 2026-04-14

ApplicantIconic Solutions by Murcia, SL
Decision Date2026-04-14
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Inbentus Versatile is a medical device manufactured by Iconic Solutions by Murcia, SL. It received FDA 510(k) clearance on 2026-04-14 under approval number K252663. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Inbentus Versatile?

Inbentus Versatile is a medical device that received FDA 510(k) clearance on 2026-04-14. It is manufactured by Iconic Solutions by Murcia, SL. The 510(k) number is K252663.

When was Inbentus Versatile approved by the FDA?

Inbentus Versatile received FDA 510(k) clearance on 2026-04-14, under approval number K252663.

What company makes Inbentus Versatile?

Inbentus Versatile is manufactured by Iconic Solutions by Murcia, SL.

What is the FDA product code for Inbentus Versatile?

The FDA product code for Inbentus Versatile is CBK.

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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.

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