Eywa Srl
ItalyFDA 510(k) applicant, unverified
- Devices
- 2
What Eywa Srl makes
Eywa Srl manufactures the Limfa Therapy System, a device designed for lymphatic drainage therapy. This system is intended for use in medical settings to assist in reducing fluid accumulation and promoting lymphatic flow in patients.
The Limfa Therapy System is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- GUDID
Limfa Therapy System (Limfa Therapy) Ref K243165
510(k) 510(k)
Company details
- DUNS number
- 431064194
Frequently asked questions
How many devices does Eywa Srl have in the registry?
The registry currently lists 2 devices for Eywa Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eywa Srl's devices?
Among its 2 most recently registered devices, Eywa Srl has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Eywa Srl's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eywa Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eywa Srl in the registry?
The most recently registered devices listed for Eywa Srl include Limfa Therapy System (Limfa Therapy) LMF000THR and Limfa Therapy System (Limfa Therapy).