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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 a medical device manufactured by ArthroCare Corporation. It received FDA 510(k) clearance on 2026-03-25 under approval 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. It is manufactured by ArthroCare Corporation. The 510(k) number is K253680.

When was LYNX COBLATION Laryngeal Wand (72290254) approved by the FDA?

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

What company makes LYNX COBLATION Laryngeal Wand (72290254)?

LYNX COBLATION Laryngeal Wand (72290254) is manufactured by ArthroCare Corporation.

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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