Data / Medical devices / Transducer, Ultrasonic, Diagnostic / France
FDA-registered makers of Transducer, Ultrasonic, Diagnostic in France: 11 establishments
11 establishments in France are registered with the FDA to make Transducer, Ultrasonic, Diagnostic (product code ITX). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Transducer, Ultrasonic, Diagnostic
- Product code
- ITX
- Country
- France
Makers of Transducer, Ultrasonic, Diagnostic in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Koelis | MEYLAN Isere, France | Manufacturer | 3 | July 10, 2018 | 0 | 0 | 0 | api.fda.gov |
| Adechotech | NAVEIL Loir-et-Cher, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Araymondlife | Voreppe Isere, France | Contract 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 | |
| Echosens | Paris, France | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Echosens Creteil | Creteil Val-de-Marne, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Parallel Design SAS | Valbonne, France | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quantel Medical | COURNON AUVERGNE Puy-de-Dome, France | 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 | |
| Westlake Plastics Europe | TOURCOING Nord, 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.