Data / Medical devices / United Kingdom / Haymax Limited
Haymax Limited: FDA-registered device maker in Conwy Gwynedd, United Kingdom, 1 510(k) clearance
Haymax Limited is registered with the FDA (registration 3010053755) in Conwy Gwynedd, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 17, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010053755
- Address
- Unit 10a Conwy Morfa Enterprise Park; Parc Caer Seion, Conwy Gwynedd, United Kingdom, LL32 8FA
- Owner or operator
- HayMax Limited (10042550)
- Roles
- Specification developer
- First device listed
- December 7, 2012
- Registered through
- 2026
- Brand names listed
- HayMax Aloe Vera, HayMax Lavender, HayMax Original, HayMax Pure
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cream, Nasal, Topical, Mechanical Allergen Particle Barrier | NUP | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 17, 2012 | K120894 | HAYMAX | NUP | Substantially Equivalent | Haymax Limited | accessdata.fda.gov |
Compare with other makers
Updated May 17, 2012. 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.