# K113118: Stentube Lacrimal Intubation Set

- Pathway: 510(k) (Special)
- Applicant: Quest Medical, Inc.
- Decided: Jul 31, 2012 after 284 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: 1 generation back to K962151 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K962151: Ryder Lacrimal Intubationset, Ryder Intl. Corp. (1996) Summary page 1.

## Indications for use
The STENTube Lacrimal Intubation Set is indicated for the following: 1. Maintenance of lacrimal outflow post-primary DCR surgical procedure 2. Maintenance of lacrimal outflow post-failed open OCR surgical procedures with complete obstruction 3. Reconstruction of the canaliculi

Source page: https://510kreport.com/device/K113118
Methodology: https://510kreport.com/methodology