# K160710: Oasis Lacrimal Intubation Set

- Pathway: 510(k) (Traditional)
- Applicant: Anodyne
- Decided: May 13, 2016 after 59 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: 2 generations back to K991238 (1999). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121142: Crawford Biocanaliculus Intubation, Fci Sas (France Chirurgie Instrumentation) (2012) Summary page 4.
- (no number) Crawford Hook: named in the summary without a submission number

## Indications for use
The Oasis Medical Lacrimal Intubation Set is intended for use for nasolacrimal intubation in patients 12 months of age and older. Indications for nasolacrimal intubation performed with the Oasis Medical Lacrimal Intubation device are: Canalicular pathologies (e.g.. congenital or acquired stenosis. lacerations) During dacryocystorhinostomy Congenital lacrimal duct obstruction

Source page: https://510kreport.com/device/K160710
Methodology: https://510kreport.com/methodology