Haymax Limited
United KingdomFDA applicant, unverified FDA FEI 3010053755
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Haymax Limited makes
Haymax Limited manufactures the HAYMAX device, a medical solution designed for the management of nasal congestion and sinus drainage, typically used in clinical settings to facilitate breathing and reduce nasal obstruction.
The HAYMAX device is classified as a Class II medical device in the United States and is listed under the FDA’s 510(k) pathway. The company is based in the US.
Catalogue
Haymax Ref K120894
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010053755
- Address
- Unit 10a, Conwy Gwynedd
Frequently asked questions
How many devices does Haymax Limited have in the registry?
The registry currently lists 1 device for Haymax Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Haymax Limited's devices?
Among its 1 most recently registered device, Haymax Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Haymax Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Haymax Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Haymax Limited in the registry?
The most recently registered devices listed for Haymax Limited include HAYMAX.