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FDA 510(k)

FLOW FLEXTEND Wand (72290039)

K-Number: K254122 · 2026-03-30

ApplicantArthroCare Corporation
Decision Date2026-03-30
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLOW FLEXTEND Wand (72290039) is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-30 under 510(k) number K254122. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW FLEXTEND Wand (72290039)?

FLOW FLEXTEND Wand (72290039) is a medical device that received FDA 510(k) clearance on 2026-03-30. The listed applicant is ArthroCare Corporation. The 510(k) number is K254122.

When did FLOW FLEXTEND Wand (72290039) receive FDA 510(k) clearance?

FLOW FLEXTEND Wand (72290039) received FDA 510(k) clearance on 2026-03-30, under 510(k) number K254122.

Who is the listed applicant for FLOW FLEXTEND Wand (72290039)?

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

What is the FDA product code for FLOW FLEXTEND Wand (72290039)?

The FDA product code for FLOW FLEXTEND Wand (72290039) is GEI.

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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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