# K211250: VisionPort System

- Pathway: 510(k) (Traditional)
- Applicant: New View Surgical, Inc.
- Decided: Jun 21, 2021 after 56 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 K923982 (1993). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161838: Xenocor Xenoscope Laparoscopic System, Xenocor, Inc. (2016) Summary page 4.
- K122511: Endopath Xcel Bladeless Trocar with Optiview Technology Endopath Xcel Blunt Tip Trocar with Optiview Technology Endopath, Ethicon Endo-Surgery, LLC (2012) Summary page 4.

## Most influential descendants
- K241502: P-Scope (2024), 0 descendants of its own

## Indications for use
The VisionPort System is intended to be used in diagnostic and therapeutic procedures for endoscopic surgery within the thoracic and peritoneal cavities including the female reproductive organs to establish a path of entry for endoscopic instruments and to provide an image of the surgical field. The trocar may be used with or without visualization for primary and secondary insertions.

Source page: https://510kreport.com/device/K211250
Methodology: https://510kreport.com/methodology