Data / Medical devices / Nebulizer (Direct Patient Interface) / United Kingdom
FDA-registered makers of Nebulizer (Direct Patient Interface) in the United Kingdom: 5 establishments
5 establishments in the United Kingdom are registered with the FDA to make Nebulizer (Direct Patient Interface) (product code CAF). 3 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
- Nebulizer (Direct Patient Interface)
- Product code
- CAF
- Country
- United Kingdom
Makers of Nebulizer (Direct Patient Interface) in the United Kingdom
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ConvaTec Limited, GDC Building | Deeside Flintshire, United Kingdom | Specification developer | 1 | September 7, 1979 | 0 | 0 | 0 | api.fda.gov |
| Flexicare Medical Ltd. | RHONDDA CYNON TAFF Wales, United Kingdom | Specification developer | 1 | July 1, 2011 | 0 | 0 | 0 | api.fda.gov |
| Intersurgical Ltd. | Wokingham, Berkshire, United Kingdom | Specification developer | 1 | October 23, 1991 | 0 | 0 | 0 | api.fda.gov |
| Cogent Technology Limited | Felixstowe Suffolk, United Kingdom | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vectura Group LTD | Chippenham Wiltshire, United Kingdom | 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.