Vivi S.R.L.
ItalyFDA 510(k) applicant, unverified
- Devices
- 1
What Vivi S.R.L. makes
Vivi S.R.L. manufactures the VIVI ERGON-X HF, a high-frequency electrotherapy device designed for muscle stimulation and rehabilitation applications.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US regulatory registry.
Catalogue
Vivi Ergon-X Hf Ref K120318
510(k) 510(k)
Frequently asked questions
How many devices does Vivi S.R.L. have in the registry?
The registry currently lists 1 device for Vivi S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vivi S.R.L.'s devices?
Among its 1 most recently registered device, Vivi S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Vivi S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vivi S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vivi S.R.L. in the registry?
The most recently registered devices listed for Vivi S.R.L. include VIVI ERGON-X HF.