Data / Medical devices / Material, Impression / Italy
FDA-registered makers of Material, Impression in Italy: 5 establishments
5 establishments in Italy are registered with the FDA to make Material, Impression (product code ELW). 5 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
- Material, Impression
- Product code
- ELW
- Country
- Italy
Makers of Material, Impression in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Zhermack S.P.A. | BADIA POLESINE (RO) Rovigo, Italy | Contract manufacturer, Manufacturer | 14 | March 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Kerr Italia, S.r.l. | SCAFATI Salerno, Italy | Manufacturer | 7 | May 30, 2013 | 0 | 0 | 0 | api.fda.gov |
| La.sc.od. SPA | FLORENCE, TUSCANY Firenze, Italy | Manufacturer | 2 | May 5, 2020 | 0 | 0 | 0 | api.fda.gov |
| Major Prodotti Dentari S.P.A. | MONCALIERI Torino, Italy | Manufacturer | 1 | October 29, 1996 | 0 | 0 | 0 | api.fda.gov |
| Vannini Dental Industry SRL | GRASSINA(FI) Firenze, Italy | Manufacturer | 1 | November 14, 1996 | 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.