Data / Medical devices / Spain / Intermedic Arfran, S.A.
Intermedic Arfran, S.A.: FDA-registered device maker in Cerdanyola del Valles Barcelona, Spain, 2 510(k) clearances
Intermedic Arfran, S.A. is registered with the FDA (registration 3008206114) in Cerdanyola del Valles Barcelona, Spain. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 4, 2009. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008206114
- Address
- C/ Boters, 8-10 Parc Tecnologic del Valles, Cerdanyola del Valles Barcelona, Spain, 08290
- Owner or operator
- INTERMEDIC ARFRAN, S.A. (9080859)
- Roles
- Manufacturer
- First device listed
- September 12, 2006
- Registered through
- 2026
- Brand names listed
- Intermedic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 |
|---|---|---|---|---|---|---|
| June 4, 2009 | K091323 | MODIFIED INTERMEDIC DIODE LASER 980NM SYSTEM (MULTIDIODE SST 200) | GEX | Substantially Equivalent | Intermedic Arfran, SA | accessdata.fda.gov |
| September 6, 2006 | K053540 | INTERMEDIC DIODE LASER FAMILY 810NM AND 980NM (AND THE DELIVERY ACCESSORIES THAT ARE USED WITH THEM TO DELIVER LASER ENE | GEX | Substantially Equivalent | Intermedic Arfran, SA | accessdata.fda.gov |
Compare with other makers
Updated June 4, 2009. 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.