# K232042: NexPort™ Trocar System (TS211001); NexPort™ Trocar System (TS211002); NexPort™ Trocar System (TS211003); NexPort™ Trocar System (TS211010); NexPort™ Trocar System (TS211011); NexPort™ Trocar System (TS211012); NexPort™ Trocar System (TS221001); NexPort™ Trocar System (TS221002); NexPort™ Trocar System (TS221003); NexPort™ Trocar System (TS221010); NexPort™ Trocar System (TS221011); NexPort™ Trocar System (TS221012); NexPort™ Trocar System (TS221020); NexPort™ Trocar System (TS221021);

- Pathway: 510(k) (Traditional)
- Applicant: Mediconcepts Technology (Shenzhen) Company Limited
- Decided: Oct 20, 2023 after 102 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: 3 generations back to K032676 (2003). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201641: Disposable Laparoscope Trocar, Beijing Biosis Healing Biolog Ical Technology Co., Ltd. (2020) Summary page 6.
- K180208: Disposable Endoscopic Trocar, Fengh Medical Co., Ltd. (2018) Summary page 6.

## Indications for use
This device is a sterile, single-use device and indicated for use in general, thoracic, gynecologic, or minimally invasive procedures to establish a path of entry for minimally invasive instruments.

Source page: https://510kreport.com/device/K232042
Methodology: https://510kreport.com/methodology