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FDA 510(k)

Any-Paste

K-Number: K253167 · 2026-01-12

ApplicantMediclus Co., Ltd.
Decision Date2026-01-12
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Any-Paste is a medical device manufactured by Mediclus Co., Ltd.. It received FDA 510(k) clearance on 2026-01-12 under approval number K253167. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Any-Paste?

Any-Paste is a medical device that received FDA 510(k) clearance on 2026-01-12. It is manufactured by Mediclus Co., Ltd.. The 510(k) number is K253167.

When was Any-Paste approved by the FDA?

Any-Paste received FDA 510(k) clearance on 2026-01-12, under approval number K253167.

What company makes Any-Paste?

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

What is the FDA product code for Any-Paste?

The FDA product code for Any-Paste is KIF.

Other Devices by Mediclus Co., Ltd.

K230465Hi-Bond Universal K241147Any-Com K232182One-Fil K252465Any-Core K251884One-Fil Putty Injectable K251283Once-Fil 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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