Data / Medical devices / Italy / Media Lab S.P.A.
Media Lab S.P.A.: FDA-registered device maker in Follo La Spezia, Italy, 1 510(k) clearance
Media Lab S.P.A. is registered with the FDA (registration 3001106601) in Follo La Spezia, Italy. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 25, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3001106601
- Address
- Via Trieste 4, Follo La Spezia, Italy, 19020
- Owner or operator
- MEDIA LAB S.P.A. (10051314)
- Roles
- Manufacturer
- First device listed
- March 2, 2016
- Registered through
- 2026
- Brand names listed
- IMPLANT 3D, Neoplan, Neoplan Viewer, Zinic 3D
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| February 25, 2016 | K153091 | IMPLANT 3D | LLZ | Substantially Equivalent | Media Lab S.R.L. | accessdata.fda.gov |
Compare with other makers
Updated February 25, 2016. 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.