# K252532: Inno-Port Disposable Bladed Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Taiwan Surgical Corporation
- Decided: Jun 2, 2026 after 294 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K011257 (2001). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151548: VersaOne Bladed Trocar, VersaOne Bladeless Trocar, Covidien (2015) Summary page 5.
- K152149: VersaOne Bladed Trocar 5mm, Covidien (2016) Summary page 5.

## Indications for use
The Inno-Port Disposable Bladed Trocars are intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry.

Source page: https://510kreport.com/device/K252532
Methodology: https://510kreport.com/methodology