Data / Medical devices / Italy / La.sc.od. SPA
La.sc.od. SPA: FDA-registered device maker in FLORENCE, TUSCANY Firenze, Italy, 2 510(k) clearances
La.sc.od. SPA is registered with the FDA (registration 8021059) in FLORENCE, TUSCANY Firenze, Italy. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 5, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8021059
- FEI number
- 3007746785
- Address
- Via Longo, 18 Sesto Fiorentino, FLORENCE, TUSCANY Firenze, Italy, 50019
- Owner or operator
- LA.SC.OD. SPA (8021059)
- Roles
- Manufacturer
- First device listed
- February 14, 1995
- Registered through
- 2026
- Brand names listed
- Alginelle, Alginor, Algisyr, Exploit, Ghenesyl Body Heavy Fast Set, Ghenesyl Body Heavy Normal Set, Ghenesyl Body Light Fast Set, Ghenesyl Body Light Normal Set and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Handle, Instrument, Dental | EJB | 1 | Manufacturer | accessdata.fda.gov |
| Material, Impression | ELW | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Restorative And Impression Material | EID | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Impression, Preformed | EHY | 1 | 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 |
|---|---|---|---|---|---|---|
| May 5, 2020 | K201184 | Lascod Impression Materials | ELW | Substantially Equivalent | Lascod Spa | accessdata.fda.gov |
| August 23, 2012 | K121824 | ALGINOR ALGINELLE TYPE 1 AND 2 MILLENIUM KROMOPAN 1 AND 2 | ELW | Substantially Equivalent | Lascod Spa | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Restorative And Impression Material
- All makers of Material, Impression
- All makers of Handle, Instrument, Dental
- All makers of Tray, Impression, Preformed
Updated May 5, 2020. 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.