Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Threadstone, LLC. It received FDA 510(k) clearance on 2026-03-23 under 510(k) 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. The listed applicant is Threadstone, LLC. The 510(k) number is K254275.

When did HyperSuture All Green Extension Line receive FDA 510(k) clearance?

HyperSuture All Green Extension Line received FDA 510(k) clearance on 2026-03-23, under 510(k) number K254275.

Who is the listed applicant for HyperSuture All Green Extension Line?

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

What is the FDA product code for HyperSuture All Green Extension Line?

The FDA product code for HyperSuture All Green Extension Line is GAT.

Other records listing Threadstone, LLC 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.

K242201HyperSuture White/Green Extension LineK241376HyperSuture All Blue Extension LineK234079HyperSuture Extension LineK230311HyperSuture

Related Devices (Code: GAT)

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.

K261021EasyWhip FamilyWinter Innovations, Inc.K260775Polyethylene;Polyethylene Fusion;Polyethylene OrthoTape™Teleflex Medical, LLCK254188Meniscus VersaflexGM Dos Reis Industria e Comercio Ltda.K253145Pre-Sutured TendonRti Surgical, Inc.K253024ProZip Knotless ImplantRiverpoint MedicalK252225PowerKnot High Strength SuturesMedacta International S.A.

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.

↑