Amferia AB
SwedenFDA applicant, unverified
- Devices
- 1
What Amferia AB makes
Amferia AB manufactures the Amferia Wound Dressing, a medical device designed for wound care applications to support healing and protect against infection.
The company’s wound dressing is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Amferia Wound Dressing Ref DEN250006
Regimes: De Novo Registry: De Novo
Frequently asked questions
How many devices does Amferia AB have in the registry?
The registry currently lists 1 device for Amferia AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Amferia AB's devices?
Among its 1 most recently registered device, Amferia AB has devices listed in FDA 510(k) (1 device).
What risk classes do Amferia AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Amferia AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Amferia AB in the registry?
The most recently registered devices listed for Amferia AB include Amferia Wound Dressing.