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FDA 510(k)

Any-Core

K-Number: K252465 · 2025-12-05

ApplicantMediclus Co., Ltd.
Decision Date2025-12-05
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Any-Core is a medical device manufactured by Mediclus Co., Ltd.. It received FDA 510(k) clearance on 2025-12-05 under approval number K252465. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Any-Core?

Any-Core is a medical device that received FDA 510(k) clearance on 2025-12-05. It is manufactured by Mediclus Co., Ltd.. The 510(k) number is K252465.

When was Any-Core approved by the FDA?

Any-Core received FDA 510(k) clearance on 2025-12-05, under approval number K252465.

What company makes Any-Core?

Any-Core is manufactured by Mediclus Co., Ltd..

What is the FDA product code for Any-Core?

The FDA product code for Any-Core is EBF.

Other Devices by Mediclus Co., Ltd.

K230465Hi-Bond Universal K241147Any-Com K232182One-Fil K251884One-Fil Putty Injectable K251283Once-Fil Flow K250823Any-Com Flow

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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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