Data / Medical devices / Italy / Vannini Dental Industry SRL
Vannini Dental Industry SRL: FDA-registered device maker in GRASSINA(FI) Firenze, Italy, 1 510(k) clearance
Vannini Dental Industry SRL is registered with the FDA (registration 8021038) in GRASSINA(FI) Firenze, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 14, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8021038
- FEI number
- 7209
- Address
- Via Di Campigliano 55/A, GRASSINA(FI) Firenze, Italy, 50015
- Owner or operator
- VANNINI DENTAL INDUSTRY SRL (8021038)
- Roles
- Manufacturer
- First device listed
- October 27, 2014
- Registered through
- 2026
- Brand names listed
- Cromatic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Material, Impression | ELW | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 14, 1996 | K963609 | PHASE PLUS | ELW | Substantially Equivalent | Zhermack S.P.A. | accessdata.fda.gov |
Compare with other makers
Updated November 14, 1996. 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.