FDA 510(k)

CephNinja

K-Number: K241819 · 2025-01-23

Decision Date2025-01-23

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

CephNinja is the device name listed in this FDA 510(k) record. The listed applicant is Cyncronus, LLC. It received FDA 510(k) clearance on 2025-01-23 under 510(k) number K241819. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CephNinja?

CephNinja is a medical device that received FDA 510(k) clearance on 2025-01-23. The listed applicant is Cyncronus, LLC. The 510(k) number is K241819.

When did CephNinja receive FDA 510(k) clearance?

CephNinja received FDA 510(k) clearance on 2025-01-23, under 510(k) number K241819.

Who is the listed applicant for CephNinja?

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

What is the FDA product code for CephNinja?

The FDA product code for CephNinja is LLZ.

Related Devices (Code: LLZ)

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.

K262449AdvaViewADVAHEALTH SOLUTIONS, LLC K261916NeuroQuant PETCortechs Labs, Inc.K260936RadioViewAINeurocareai, Inc. (Dba Savelife.Ai)K260588Cleerly LABSCleerly, Inc.K262462TheraSphere 360™ Y-90 Management PlatformBoston Scientific Corporation K262143ImageGrid StreamVueCandelis, Inc.

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.