Data / Medical devices / Cannula, Ophthalmic / United Kingdom
FDA-registered makers of Cannula, Ophthalmic in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Cannula, Ophthalmic (product code HMX). 0 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
- Cannula, Ophthalmic
- Product code
- HMX
- Country
- United Kingdom
Makers of Cannula, Ophthalmic in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Altomed Ltd. | Boldon Colliery South Tyneside, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beaver-Visitec International, Ltd | BIDFORD-ON-AVON Warwickshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Blink Medical LTD | Solihull, United Kingdom | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Duckworth & Kent, Ltd. | BALDOCK Hertfordshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sterimedix Ltd. | REDDITCH Worcestershire, United Kingdom | Contract manufacturer, 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.