# K152149: VersaOne Bladed Trocar 5mm

- Pathway: 510(k) (Special)
- Applicant: Covidien
- Decided: Jan 22, 2016 after 172 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.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062326: Autosuture Modified Versaport Trocar with Fixation Sleeve, United States Surgical, A Division of Tyco Healthc (2006) Summary page 4.
- K112349: Versaport V2 Bladeless Optiical Trocar and/or Versaport Bladeless Optical Trocar, Covidien, Formerly US Surgical A Divison of Tyco H (2011) Summary page 4.

## Most influential descendants
- K252532: Inno-Port Disposable Bladed Trocar (2026), 0 descendants of its own

## Indications for use
indicated for use in a variety of gynecologic, general, thoracic, and urologic endoscopic procedures to create and maintain a port of entry.

Source page: https://510kreport.com/device/K152149
Methodology: https://510kreport.com/methodology