Data / Medical devices / Accessories, Implant, Dental, Endosseous / Italy
FDA-registered makers of Accessories, Implant, Dental, Endosseous in Italy: 11 establishments
11 establishments in Italy are registered with the FDA to make Accessories, Implant, Dental, Endosseous (product code NDP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Accessories, Implant, Dental, Endosseous
- Product code
- NDP
- Country
- Italy
Makers of Accessories, Implant, Dental, Endosseous in Italy
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 3diemme SRL | Cantu Como, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Den Tag S.R.L. | MANIAGO, PN. Pordenone, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ivoclar Vivadent Manufacturing GmbH | NATURNO (BZ) Bolzano, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| J Dental Care SRL | Modena, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leone SPA | Sesto Fiorentino Firenze, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mectron S.P.A. | CARASCO Genova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDESY srl | MANIAGO Pordenone, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nobil-Metal S P A | Villafranca Dasti, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Rhein 83 SRL | BOLOGNA Emilia-Romagna, Italy | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sweden & Martina S.P.A. | Due Carrare Padova, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zirkonzahn SRL | Gais Bolzano, Italy | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.