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FDA 510(k)

CHIKAI Nexus petit

K-Number: K252011 · 2026-02-02

Decision Date2026-02-02
Product CodeMOF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHIKAI Nexus petit is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2026-02-02 under 510(k) number K252011. The device is classified under product code MOF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHIKAI Nexus petit?

CHIKAI Nexus petit is a medical device that received FDA 510(k) clearance on 2026-02-02. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K252011.

When did CHIKAI Nexus petit receive FDA 510(k) clearance?

CHIKAI Nexus petit received FDA 510(k) clearance on 2026-02-02, under 510(k) number K252011.

Who is the listed applicant for CHIKAI Nexus petit?

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

What is the FDA product code for CHIKAI Nexus petit?

The FDA product code for CHIKAI Nexus petit is MOF.

Other records listing Asahi Intecc 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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Related Devices (Code: MOF)

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.

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.