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FDA 510(k)

V-soft Line™ Barbed Surgical Suture (Various)

K-Number: K250107 · 2025-10-15

ApplicantFeeltech Co., Ltd.
Decision Date2025-10-15
Product CodeNEW
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

V-soft Line™ Barbed Surgical Suture (Various) is the device name listed in this FDA 510(k) record. The listed applicant is Feeltech Co., Ltd.. It received FDA 510(k) clearance on 2025-10-15 under 510(k) number K250107. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-soft Line™ Barbed Surgical Suture (Various)?

V-soft Line™ Barbed Surgical Suture (Various) is a medical device that received FDA 510(k) clearance on 2025-10-15. The listed applicant is Feeltech Co., Ltd.. The 510(k) number is K250107.

When did V-soft Line™ Barbed Surgical Suture (Various) receive FDA 510(k) clearance?

V-soft Line™ Barbed Surgical Suture (Various) received FDA 510(k) clearance on 2025-10-15, under 510(k) number K250107.

Who is the listed applicant for V-soft Line™ Barbed Surgical Suture (Various)?

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

What is the FDA product code for V-soft Line™ Barbed Surgical Suture (Various)?

The FDA product code for V-soft Line™ Barbed Surgical Suture (Various) is NEW.

Related Clinical Trials

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.

NCT07491276Efficacy of Using Knotless Barbed Suture vs N-Butyl Cyanoacrylate Glue Tissue Adhesive for Closure of Intraoral Surgical IncisionsACTIVE_NOT_RECRUITING

Other records listing Feeltech Co., Ltd. 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.

K251414Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)K213010FEELject LDV (Low dead volume) syringeK172602Miracu

Related Devices (Code: NEW)

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.

K261988Monodek™ (POLYDIOXANONE) Dyed Violet Monofilament Synthetic Absorbable Surgical SutureTeleflex Medical, LLCK252171Barbed PDO SutureSutura Medical Technology, Inc.K252047STRATAFIX™ Symmetric PDS™ Plus Knotless Tissue Control DevicesETHICON, Inc.K243897PDS™ Plus Antibacterial (Polydioxanone) Sterile Synthetic Absorbable Surgical SutureETHICON, Inc.K251414Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)Feeltech Co., Ltd.K252644PINION™ PDO Knotless Suture - Absorbable Poly (P-Dioxanone) Knotless Suture; PINION™ PGA-PCL Knotless Suture - Absorbable Poly (Glycolide-Co-Caprolactone) Knotless SutureM/s. Meril Endo Surgery Private Limited.

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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