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FDA 510(k)

cCeLL405

K-Number: K254030 · 2026-10-02

ApplicantVPIX Medical, Inc.
Decision Date2026-10-02
Product CodeQFX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

cCeLL405 is the device name listed in this FDA 510(k) record. The listed applicant is VPIX Medical, Inc.. It received FDA 510(k) clearance on 2026-10-02 under 510(k) number K254030. The device is classified under product code QFX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the cCeLL405?

cCeLL405 is a medical device that received FDA 510(k) clearance on 2026-10-02. The listed applicant is VPIX Medical, Inc.. The 510(k) number is K254030.

When did cCeLL405 receive FDA 510(k) clearance?

cCeLL405 received FDA 510(k) clearance on 2026-10-02, under 510(k) number K254030.

Who is the listed applicant for cCeLL405?

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

What is the FDA product code for cCeLL405?

The FDA product code for cCeLL405 is QFX.

Related Clinical Trials

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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Other records listing VPIX Medical, Inc. 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.

K251852cCeLL - In vivo with Drop-In Robo (CN100-2W2C488775, CN100-1W1C775, DR200)K233391cCeLL - In vivo

Related Devices (Code: QFX)

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.

K251286Affirm 400Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K240215BLUE 400; BLUE 400 SCarl Zeiss Meditec, AGK232567Myriad SPECTRA Light SourceNico CorporationK211346BLUE 400Carl Zeiss Meditec, AG

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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