# K092584: Laport

- Pathway: 510(k) (Traditional)
- Applicant: Mgb Endoskopische Gerate GmbH (Berlin)
- Decided: Mar 22, 2010 after 210 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K171741: Laport (2017), 1 descendant of its own
- K252985: Laport (2026), 0 descendants of its own

## Indications for use
The MGB LAPORT sterile Trocars for Endloscopic surgery are intended to establish a path of entry for endloscopic instruments for use during general, abdominal, gynaecological and thoracic minimally invasive procedures or to gain access through tissue planes and/or potential spaces for endloscopic instruments.

Source page: https://510kreport.com/device/K092584
Methodology: https://510kreport.com/methodology