# K252985: Laport

- Pathway: 510(k) (Traditional)
- Applicant: Sejong Medical Co., Ltd.
- Decided: May 19, 2026 after 243 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: 2 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)
- K171741: Laport, Sejong Medical Co., Ltd. (2017) Summary page 5.

## Indications for use
Laport Trocars have applications in abdominal, thoracic, and gynecologic minimally invasive procedures to establish a path of entry for endoscopic instruments.

Source page: https://510kreport.com/device/K252985
Methodology: https://510kreport.com/methodology