CHIKAI Nexus petit
K-Number: K252011 · 2026-02-02
Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.