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FDA 510(k)

CyClean Cord

K-Number: K254239 · 2026-03-27

ApplicantSS GLOBAL
Decision Date2026-03-27
Product CodeMVL
DecisionSubstantially Equivalent

Device Summary

CyClean Cord is the device name listed in this FDA 510(k) record. The listed applicant is SS GLOBAL. It received FDA 510(k) clearance on 2026-03-27 under 510(k) number K254239. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CyClean Cord?

CyClean Cord is a medical device that received FDA 510(k) clearance on 2026-03-27. The listed applicant is SS GLOBAL. The 510(k) number is K254239.

When did CyClean Cord receive FDA 510(k) clearance?

CyClean Cord received FDA 510(k) clearance on 2026-03-27, under 510(k) number K254239.

Who is the listed applicant for CyClean Cord?

The FDA 510(k) record lists SS GLOBAL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CyClean Cord?

The FDA product code for CyClean Cord is MVL.

Related Devices (Code: MVL)

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.

K253797One-StopMediclus Co., Ltd.K243910RetraxilKulzer, LLCK211420Stasis GelBelport Company, Inc., Gingi-PakK211419Gingi-Aid GelBelport Company, Inc., Gingi-PakK213149VOCO Retraction PasteVoco GmbHK200764STATSTIXCentrix Incorporated

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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