Elesta S.p.A.
ItalyFDA applicant, unverified
- Devices
- 2
What Elesta S.p.A. makes
Elesta S.P.A makes the ECHOLASER X4, which is a laser-based medical device used for therapeutic or diagnostic applications.
The ECHOLASER X4 is classified as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Echolaser X4 Ref K261964
Regimes: 510(k) Registry: 510(k)Echolaser X4 Ref K213594
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Elesta S.P.A have in the registry?
The registry currently lists 2 devices for Elesta S.P.A. Devices recorded under merged duplicate company entries are counted once.
Which registries list Elesta S.P.A's devices?
Among its 2 most recently registered devices, Elesta S.P.A has devices listed in FDA 510(k) (2 devices).
What risk classes do Elesta S.P.A's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Elesta S.P.A's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Elesta S.P.A in the registry?
The most recently registered devices listed for Elesta S.P.A include ECHOLASER X4.