# K252714: C-Lant Port

- Pathway: 510(k) (Traditional)
- Applicant: Vigor Medical Technologies, Ltd.
- Decided: Feb 27, 2026 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: 5 generations back to K990028 (1999). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211577: SoftFix Balloon Trocar, Unimax Medical Systems, Inc. (2021) Summary page 5.
- K150549: Reactor (TM) Trocar and Sleeve, Sharp Medical Prducts, LLC (2015) Summary page 5.
- K083638: Fixation Trocars, Applied Medical Resources Corp. (2008) Summary page 5.

## Indications for use
The C-Lant Port is intended for use in a variety of endoscopic procedures to provide a port of entry into the abdominal and thoracic cavities.

Source page: https://510kreport.com/device/K252714
Methodology: https://510kreport.com/methodology