# K130435: Versaport V2 Bladeless Optical Trocar

- Pathway: 510(k) (Special)
- Applicant: Covidien, Formerly US Surgical A Divison of Tyco H
- Decided: Mar 14, 2013 after 21 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 K011257 (2001). 4 ancestors in all.
11 later devices descend from it; 7 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112349: Versaport V2 Bladeless Optiical Trocar and/or Versaport Bladeless Optical Trocar, Covidien, Formerly US Surgical A Divison of Tyco H (2011) Summary page 1.
- K081169: Autosuture Versaport Plus Bladless Trocar; Bladeless Trocar, Covidien Lp, Formerly Registered AS United States (2008) Summary page 1.

## Most influential descendants
- K151548: VersaOne Bladed Trocar, VersaOne Bladeless Trocar (2015), 7 descendants of its own
- K163654: VersaOne fascial closure system bladed trocar, VersaOne fascial closure system bladeless trocar, VersaOne fascial closure system optical trocar (2017), 1 descendant of its own
- K160564: TroClose1200 (2016), 1 descendant of its own
- K162584: VersaOne Bladeless Trocar (2016), 1 descendant of its own
- K252532: Inno-Port Disposable Bladed Trocar (2026), 0 descendants of its own

## Indications for use
The Versaport T m Bladeless Optical Trocar is intended for use in a variety of gynecologic, general, thoracic and urologic endoscopic procedures to create and maintain a port of entry. The trocar may be used with or without visualization for primary and secondary insertions.

Source page: https://510kreport.com/device/K130435
Methodology: https://510kreport.com/methodology