HyperSuture All Green Extension Line
K-Number: K254275 · 2026-03-23
ApplicantThreadstone, LLC
Decision Date2026-03-23
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
HyperSuture All Green Extension Line is a medical device manufactured by Threadstone, LLC. It received FDA 510(k) clearance on 2026-03-23 under approval number K254275. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the HyperSuture All Green Extension Line?
HyperSuture All Green Extension Line is a medical device that received FDA 510(k) clearance on 2026-03-23. It is manufactured by Threadstone, LLC. The 510(k) number is K254275.
When was HyperSuture All Green Extension Line approved by the FDA?
HyperSuture All Green Extension Line received FDA 510(k) clearance on 2026-03-23, under approval number K254275.
What company makes HyperSuture All Green Extension Line?
HyperSuture All Green Extension Line is manufactured by Threadstone, LLC.
What is the FDA product code for HyperSuture All Green Extension Line?
The FDA product code for HyperSuture All Green Extension Line is GAT.
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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.