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Data / Medical devices / Italy / Telea Electronic Engineering S.R.L.

Telea Electronic Engineering S.R.L.: FDA-registered device maker in Sandrigo Vicenza, Italy, 1 510(k) clearance

Telea Electronic Engineering S.R.L. is registered with the FDA (registration 3010701628) in Sandrigo Vicenza, Italy. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 31, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3010701628
Address
via Leonardo da Vinci 13, Sandrigo Vicenza, Italy, 36066
Owner or operator
Telea Electronic Engineering S.r.l. (10046169)
Roles
Manufacturer
First device listed
February 11, 2014
Registered through
2026
Brand names listed
2501019, QUANTUM, 2501023, Vesalius MCNplus

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
January 31, 2014K131696VESALIUSGEISubstantially EquivalentTelea Electronic Engineering Srlaccessdata.fda.gov

Compare with other makers

Updated January 31, 2014. 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.