FDA 510(k)

Any-Zircos

K-Number: K262074 · 2026-08-21

Decision Date2026-08-21

Product CodeEIH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Any-Zircos is the device name listed in this FDA 510(k) record. The listed applicant is Mediclus Co., Ltd.. It received FDA 510(k) clearance on 2026-08-21 under 510(k) number K262074. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Any-Zircos?

Any-Zircos is a medical device that received FDA 510(k) clearance on 2026-08-21. The listed applicant is Mediclus Co., Ltd.. The 510(k) number is K262074.

When did Any-Zircos receive FDA 510(k) clearance?

Any-Zircos received FDA 510(k) clearance on 2026-08-21, under 510(k) number K262074.

Who is the listed applicant for Any-Zircos?

The FDA 510(k) record lists Mediclus Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Any-Zircos?

The FDA product code for Any-Zircos is EIH.

Other records listing Mediclus Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.