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FDA 510(k)

LYNX COBLATION Laryngeal Wand (72290254)

K-Number: K253680 · 2026-03-25

ApplicantArthroCare Corporation
Decision Date2026-03-25
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LYNX COBLATION Laryngeal Wand (72290254) is the device name listed in this FDA 510(k) record. The listed applicant is ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-25 under 510(k) number K253680. 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 LYNX COBLATION Laryngeal Wand (72290254)?

LYNX COBLATION Laryngeal Wand (72290254) is a medical device that received FDA 510(k) clearance on 2026-03-25. The listed applicant is ArthroCare Corporation. The 510(k) number is K253680.

When did LYNX COBLATION Laryngeal Wand (72290254) receive FDA 510(k) clearance?

LYNX COBLATION Laryngeal Wand (72290254) received FDA 510(k) clearance on 2026-03-25, under 510(k) number K253680.

Who is the listed applicant for LYNX COBLATION Laryngeal Wand (72290254)?

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 LYNX COBLATION Laryngeal Wand (72290254)?

The FDA product code for LYNX COBLATION Laryngeal Wand (72290254) 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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