Data / Medical devices / Dispenser, Liquid Medication / Italy
FDA-registered makers of Dispenser, Liquid Medication in Italy: 5 establishments
5 establishments in Italy 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.
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- Device
- Dispenser, Liquid Medication
- Product code
- KYX
- Country
- Italy
Makers of Dispenser, Liquid Medication in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cedic S.R.L. | PESCHIERA BORROMEO MILAN Lombardy, Italy | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cedic Srl Divisione Stampaggio | MIRANDOLA Modena, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dompe Farmaceutici S.P.A. | L Aquila Abruzzo, Italy | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HMC Premedical S.p.A. | MIRANDOLA Modena, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PLASTIAPE S.p.A | Osnago Lecco, Italy | Repackager or relabeler, Specification developer | 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.