# K110004: Asc Triport+ Laparoscopic Access Device

- Pathway: 510(k) (Special)
- Applicant: Advanced Surgical Concepts
- Decided: Jan 26, 2011 after 23 days
- Product code: OTJ (Laparoscopic Single Port Access Device)
- 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 K010007 (2001). 8 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101794: Asc Triport Laparoscopic Access Device Model TPRT-02-01 (WA58000T), Asc Quadport Laparoscopic Asscess Device QPRT-01 (WA, Advanced Surgical Concepts (2010) Summary page 1.

## Most influential descendants
- K121309: Asc Quadport + Laparoscopic Access Device (2012), 0 descendants of its own
- K120898: Keyport System, Includes: Keyport Silicone Sealing Insert 8850XXX Keyport Trucar 8850XX Keyport Trocar 8850XX Sealing CA (2012), 0 descendants of its own
- K111407: Triport, Triport+, TRIPORT15, Quadport (2012), 0 descendants of its own

## Indications for use
The ASC TriPort+ Laparoscopic Access Device is intended for use as a multiple instrument and/or camera port during minimally invasive abdominal laparoscopic surgery.

Source page: https://510kreport.com/device/K110004
Methodology: https://510kreport.com/methodology