# K142464: Entriport

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Mar 5, 2015 after 184 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 K924761 (1993). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073009: Oneport Surgical Trocar System, Conmed Corporation (2007) Summary page 5.

## Indications for use
The EntriPort Surgical Trocar System has applications in a variety of endoscopic procedures to provide a means of entry and access for endoscopic instruments. The Trocar may be used with or without visualization for primary and secondary insertions. The EntriPort Mini Surgical Trocar System has applications in a variety of endoscopic procedures to provide a means of entry and access for endoscopic instruments.

Source page: https://510kreport.com/device/K142464
Methodology: https://510kreport.com/methodology