Data / Medical devices / Implant, Eye Valve / United States
FDA-registered makers of Implant, Eye Valve in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Implant, Eye Valve (product code KYF). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Implant, Eye Valve
- Product code
- KYF
- Country
- United States
Makers of Implant, Eye Valve in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| New World Medical, Inc. | Rancho Cucamonga, CA, United States | Complaint file establishment, Manufacturer | 3 | May 12, 2023 | 0 | 0 | 0 | api.fda.gov |
| Johnson & Johnson Surgical Vision, Inc. | Irvine, CA, United States | Manufacturer, Specification developer | 2 | February 18, 1997 | 0 | 0 | 0 | api.fda.gov |
| Allergan Sales, LLC | Irvine, CA, United States | Complaint file establishment, Specification developer | 1 | November 21, 2016 | 0 | 1 | 0 | api.fda.gov |
| Alcon Research, LLC | Sinking Spring, PA, United States | Manufacturer | 1 | March 26, 2002 | 0 | 0 | 0 | api.fda.gov |
| Glaukos Corporation | Aliso Viejo, CA, United States | Specification developer | 1 | August 2, 2022 | 0 | 0 | 0 | api.fda.gov |
| Glaukos Corporation | San Clemente, CA, United States | Complaint file establishment, Manufacturer | 1 | August 2, 2022 | 0 | 0 | 0 | api.fda.gov |
| Trelleborg Sealing Solutions Us, Inc. | Paso Robles, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trelleborg Sealing Solutions US, Inc. | Tustin, CA, United States | Contract manufacturer | 0 | 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.