Data / Medical devices / Italy / Espansione Marketing SPA
Espansione Marketing SPA: FDA-registered device maker in FUNO Bologna, Italy, 3 510(k) clearances
Espansione Marketing SPA is registered with the FDA (registration 3006546131) in FUNO Bologna, Italy. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 19, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006546131
- Address
- Via Degli Orefici 152 Blocco 27 Centergross, FUNO Bologna, Italy, 40050
- Owner or operator
- ESPANSIONE MARKETING SPA (9098022)
- Roles
- Manufacturer
- First device listed
- June 22, 2007
- Registered through
- 2026
- Brand names listed
- EPI-C PLUS, EPI-C PLUS/E/110V, EPIC-C PLUS, EQUINOX, EVOLUZIONE PLUS, Epi-C Mask, IPL LAMP, IPL LAMP-05 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Camera, Ophthalmic, General-Use | PJZ | 2 | Manufacturer | accessdata.fda.gov |
| Laser, Comb, Hair | OAP | 2 | Manufacturer | accessdata.fda.gov |
| Light Based Over The Counter Wrinkle Reduction | OHS | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer | accessdata.fda.gov |
| Pad, Heating, Powered | IRT | 2 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| December 19, 2013 | K124064 | YOUNG AGAIN | OHS | Substantially Equivalent | Espansione Marketing S.P.A | accessdata.fda.gov |
| September 20, 2010 | K092734 | E-LIGHT LINE | GEX | Substantially Equivalent | Espansione Marketing S.P.A | accessdata.fda.gov |
| May 1, 2007 | K070494 | EPI-C PLUS | GEX | Substantially Equivalent | Espansione Marketing S.P.A | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Laser, Comb, Hair
- All makers of Massager, Therapeutic, Electric
- All makers of Camera, Ophthalmic, General-Use
- All makers of Light Based Over The Counter Wrinkle Reduction
- All makers of Pad, Heating, Powered
Updated December 19, 2013. 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.