# K140290: Stoploss Jones Tube

- Pathway: 510(k) (Traditional)
- Applicant: Ljt Surgical, Ltd.
- Decided: Dec 2, 2014 after 300 days
- Product code: OKS (Lacrimal Stents And Intubation Sets)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K883233 (1988). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113316: DCS Lacrimal Stent, Dcs Surgical, Inc. (2012) Summary page 4.
- (no number) Gunther Weiss Scientific Glassblowing Co., Inc.: Jones Tube: named in the summary without a submission number

## Indications for use
The StopLoss Jones tube system is intended for use during repair of the lacrimal system for intubation and bypass to canalicular pathologies.

Source page: https://510kreport.com/device/K140290
Methodology: https://510kreport.com/methodology