Data / Medical devices / Applicator, Absorbent Tipped, Non-Sterile / United Kingdom
FDA-registered makers of Applicator, Absorbent Tipped, Non-Sterile in the United Kingdom: 7 establishments
7 establishments in the United Kingdom are registered with the FDA to make Applicator, Absorbent Tipped, Non-Sterile (product code KXF). 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
- Applicator, Absorbent Tipped, Non-Sterile
- Product code
- KXF
- Country
- United Kingdom
Makers of Applicator, Absorbent Tipped, Non-Sterile in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Axial Medical Printing Limited | Belfast, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cell Projects Ltd | Harrietsham Kent, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Daye (anne's Day Ltd) | London London, City of, United Kingdom | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hunt Developments (uk) Limited | Midhurst West Sussex, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Wire And Equipment Co. Ltd. | Corsham, Wiltshire, United Kingdom | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Podonics, Ltd | London England, United Kingdom | Complaint file establishment, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Podopro Uk Ltd | HUDDERSFIELD England, United Kingdom | Contract manufacturer, Foreign private label distributor, Manufacturer, Repackager or relabeler | 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.