Data / Medical devices / Mouthpiece, Saliva Ejector / Italy
FDA-registered makers of Mouthpiece, Saliva Ejector in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Mouthpiece, Saliva Ejector (product code DYN). 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
- Mouthpiece, Saliva Ejector
- Product code
- DYN
- Country
- Italy
Makers of Mouthpiece, Saliva Ejector in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Asa Dental S.P.A. | MARLIA Lucca, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cefla S.C. | IMOLA Bologna, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Euronda SPA | Sandrigo Vicenza, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Larident S.R.L. | TRIBOGNA Genova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| World Work SRL | MONTEBELLO VICENTINO Vicenza, Italy | 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.