Data / Medical devices / Lacrimal Stents And Intubation Sets / United States
FDA-registered makers of Lacrimal Stents And Intubation Sets in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Lacrimal Stents And Intubation Sets (product code OKS). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Lacrimal Stents And Intubation Sets
- Product code
- OKS
- Country
- United States
Makers of Lacrimal Stents And Intubation Sets in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Katena Products, Inc. | Parsippany, NJ, United States | Specification developer | 2 | April 25, 2003 | 0 | 0 | 0 | api.fda.gov |
| Katena Products, Inc. | Randolph, NJ, United States | Specification developer | 2 | April 25, 2003 | 0 | 0 | 0 | api.fda.gov |
| Quest Medical, Inc. | Allen, TX, United States | Manufacturer | 2 | October 19, 2012 | 0 | 0 | 0 | api.fda.gov |
| Anodyne Surgical | O Fallon, MO, United States | Manufacturer | 1 | May 13, 2016 | 0 | 0 | 0 | api.fda.gov |
| Oasis Medical, Inc. | Glendora, CA, United States | Complaint file establishment, Specification developer | 1 | May 13, 2016 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.