Data / Medical devices / System, Imaging, Pulsed Echo, Ultrasonic / France
FDA-registered makers of System, Imaging, Pulsed Echo, Ultrasonic in France: 12 establishments
12 establishments in France are registered with the FDA to make System, Imaging, Pulsed Echo, Ultrasonic (product code IYO). 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
- System, Imaging, Pulsed Echo, Ultrasonic
- Product code
- IYO
- Country
- France
Makers of System, Imaging, Pulsed Echo, Ultrasonic in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Echosens | Paris, France | Manufacturer, Specification developer | 8 | July 30, 2021 | 0 | 0 | 0 | api.fda.gov |
| Echosens Creteil | Creteil Val-de-Marne, France | Manufacturer | 6 | July 30, 2021 | 0 | 0 | 0 | api.fda.gov |
| Quantel Medical | COURNON AUVERGNE Puy-de-Dome, France | Manufacturer | 6 | April 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Adechotech | NAVEIL Loir-et-Cher, France | Manufacturer | 1 | June 12, 2017 | 0 | 0 | 0 | api.fda.gov |
| Diagnoly | Lyon 3e Arrondissement Rhone, France | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| E-Scopics | Aix-en-Provence Bouches-du-Rhone, France | Complaint file establishment, Exporter to the US, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems SCS | Buc, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Koelis | MEYLAN Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Parallel Design SAS | Valbonne, France | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sonio | Paris, France | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sonoscanner Sarl | Ivry-sur-Seine Val-de-Marne, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vermon | Tours, France | Contract 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.