# K081169: Autosuture Versaport Plus Bladless Trocar; Bladeless Trocar

- Pathway: 510(k) (Special)
- Applicant: Covidien Lp, Formerly Registered AS United States
- Decided: May 23, 2008 after 29 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
No predicates in its family tree.
14 later devices descend from it; 5 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) autosuture VERSAPORT: named in the summary without a submission number
- (no number) Ethicon Excel: named in the summary without a submission number

## Most influential descendants
- K130435: Versaport V2 Bladeless Optical Trocar (2013), 11 descendants of its own
- 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

## Indications for use
The autosuture VERSAPORT PLUS Bladeless Trocar is intended 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/K081169
Methodology: https://510kreport.com/methodology