Data / Medical devices / Italy / Eywa S.R.L.
Eywa S.R.L.: FDA-registered device maker in Rimini, Italy, 1 510(k) clearance
Eywa S.R.L. is registered with the FDA (registration 3024182169) in Rimini, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 15, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3024182169
- Address
- Via Pietrarubbia 25/E, Rimini, Italy, 47922
- Owner or operator
- Eywa s.r.l. (10094368)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- November 25, 2025
- Registered through
- 2026
- Brand names listed
- LIMFA Therapy System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 15, 2025 | K243165 | Limfa Therapy System (Limfa Therapy) | NGX | Substantially Equivalent | Eywa Srl | accessdata.fda.gov |
Compare with other makers
Updated May 15, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.