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FDA 510(k)

Inno-Port Disposable Bladed Trocar

K-Number: K252532 · 2026-06-02

ApplicantTaiwan Surgical Corporation
Decision Date2026-06-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Inno-Port Disposable Bladed Trocar is the device name listed in this FDA 510(k) record. The listed applicant is Taiwan Surgical Corporation. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K252532. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Inno-Port Disposable Bladed Trocar?

Inno-Port Disposable Bladed Trocar is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is Taiwan Surgical Corporation. The 510(k) number is K252532.

When did Inno-Port Disposable Bladed Trocar receive FDA 510(k) clearance?

Inno-Port Disposable Bladed Trocar received FDA 510(k) clearance on 2026-06-02, under 510(k) number K252532.

Who is the listed applicant for Inno-Port Disposable Bladed Trocar?

The FDA 510(k) record lists Taiwan Surgical Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Inno-Port Disposable Bladed Trocar?

The FDA product code for Inno-Port Disposable Bladed Trocar is GCJ.

Other records listing Taiwan Surgical Corporation 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.

K254231Inno-Hook™ Disposable Clip Appliers (Ligating Clips) and Inno-Hook™ Ligating ClipsK253903InnoClip Disposable Clip ApplierK253781InnoClip Clip ApplierK223593Inno-Port Disposable Bladeless Trocar, Inno-Port Disposable Optical TrocarK202994InnoClip Disposable Clip Applier, InnoClip Clip Applier

Related Devices (Code: GCJ)

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.

K261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.IncK261249Universal Seal (5-12 mm)Intuitive Surgical, Inc.K260710FloShield Air System (FSS-01-1000T - 10mm, 0 Degree FloShield Air, FSS-02-1030T - 10mm, 30 Degree FloShield Air, FSS-03-1045T - 10mm, 45 Degree FloShield Air, FSS-01-0500T - 5mm, 0 Degree FloShield Air, FSS-02-0530T - 5mm, 30 Degree FloShield Air, FSS-01-0545T - 5mm, 45 Degree FloShield Air)FloShield, Inc.K260414“Tech-Image” Video Endoscope SystemTech-Image CO., LTD.

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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