# LA.SC.OD. SPA

FEI: 3007746785
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: LA.SC.OD. SPA (#8021059)

Address: VIA LONGO, 18 SESTO, FIORENTINO, FLORENCE, TUSCANY Firenze, 50019, IT

Mandatory US Agent: KROMOPAN U.S.A., INC.

## Products

Total registered: 1
Top product codes: ELW
Regulation §: 872.3660

Proprietary names: Kromopan Sil Normal Set Kit - Putty Hard + Light Body, Oklurest, Kromopan Sil Putty Soft Fast Set, Ghenesyl Putty Soft Normal Set, Kromopan Sil Mono, Ghenesyl Putty Hard Normal Set, Ghenesyl Body Light Fast Set, Ghenesyl Body Regular Normal Set, Kromopan Sil Body Super Light Normal Set, Ghenesyl Putty Soft Fast Set

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007746785%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007746785