# K962151: Ryder Lacrimal Intubationset

- Pathway: 510(k) (Traditional)
- Applicant: Ryder Intl. Corp.
- Decided: Sep 18, 1996 after 106 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
No predicates in its family tree.
2 later devices descend from it; 2 cite 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. The FDA summary names its predicate without a number.
- (no number) Concept 9035 Guibor Canaliculus Intubation Set: named in the summary without a submission number

## Most influential descendants
- K113118: Stentube Lacrimal Intubation Set (2012), 0 descendants of its own
- K973633: Atrion Medical Products Lacrimal Intubation Set (1998), 0 descendants of its own

## Indications for use
The Ryder Lacrimal Intubation set is valuable in the reconstruction of the lacrimal outflow system and also useful in canaliculus repair, lacrimal obstruction and complicated and uncomplicated dacryocystorhinostomy procedures.

Source page: https://510kreport.com/device/K962151
Methodology: https://510kreport.com/methodology