Data / Medical devices / Stimulator, Muscle, Powered, For Muscle Conditioning / Italy
FDA-registered makers of Stimulator, Muscle, Powered, For Muscle Conditioning in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Stimulator, Muscle, Powered, For Muscle Conditioning (product code NGX). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Stimulator, Muscle, Powered, For Muscle Conditioning
- Product code
- NGX
- Country
- Italy
Makers of Stimulator, Muscle, Powered, For Muscle Conditioning in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dam SRL | Cervia Ravenna, Italy | Manufacturer | 1 | March 18, 2016 | 0 | 0 | 0 | api.fda.gov |
| Domino S.R.L. | Codogne Treviso, Italy | Manufacturer | 1 | April 30, 2007 | 0 | 0 | 0 | api.fda.gov |
| El.en. Electronic Engineering SPA | CALENZANO Firenze, Italy | Manufacturer | 1 | December 19, 2023 | 0 | 0 | 0 | api.fda.gov |
| Eywa S.R.L. | Rimini, Italy | Complaint file establishment, Manufacturer | 1 | May 15, 2025 | 0 | 0 | 0 | api.fda.gov |
| Bios S.R.L. | VIMODRONE Milano, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.