Data / Medical devices / Dispenser, Liquid Medication / France
FDA-registered makers of Dispenser, Liquid Medication in France: 7 establishments
7 establishments in France are registered with the FDA to make Dispenser, Liquid Medication (product code KYX). 0 have 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
- Dispenser, Liquid Medication
- Product code
- KYX
- Country
- France
Makers of Dispenser, Liquid Medication in France
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Apothicom Distribution | Paris Ile-de-France, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cair LGL | Lissieu Rhone, France | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rovipharm | Val Revermont Ain, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sipv | Ecouen Ile-de-France, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stiplastics | Saint Marcellin Isere, France | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Union Plastic | St Didier en Velay Haute-Loire, France | Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vygon S A | ECOUEN 95440 Val-d'Oise, France | 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.