Soluscope SAS
FR-MF-000011763 · France · Aubagne
Soluscope SAS is registered in the European database on medical devices as a manufacturer, with 73 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 39 |
|---|---|
| Class IIa | 34 |
Most frequent device types declared: SL-TEE, Sl-V1-AL-PA, SL-V4-RO-PA, SL-V1-PA, SL-V1-AL-GTA.
Among these devices, 25 are declared active.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 73 |
| Country of registration | France |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.