Allergy Direct
Country not established
- Devices
- 1
What Allergy Direct makes
Allergy Direct makes allergen barriers for bedding, including mattress encasings, duvet encasings, pillow encasings, and complete bedding systems designed to reduce exposure to allergens.
These devices are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allergy Direct have in the registry?
The registry currently lists 1 device for Allergy Direct. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allergy Direct's devices?
Among its 1 most recently registered device, Allergy Direct has devices listed in FDA 510(k) (1 device).
What risk classes do Allergy Direct's devices fall under?
Among its 1 most recently registered device, the classes recorded for Allergy Direct's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Allergy Direct in the registry?
The most recently registered devices listed for Allergy Direct include EVENT ALLERGEN BARRIERS, EVENT MATTRESS ENCASING, EVENT DUVET ENCASING, EVENT PILLOW ENCASING, EVENT BEDDING SYSTEM.