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Data / Medical devices / Israel / Savion Industries (1987), Ltd.

Savion Industries (1987), Ltd.: FDA-registered device maker in ASHDOD Southern, Israel, 1 510(k) clearance

Savion Industries (1987), Ltd. is registered with the FDA (registration 9681454) in ASHDOD Southern, Israel. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 28, 2005. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9681454
FEI number
3002572935
Address
7 Hamada ST., ASHDOD Southern, Israel, 77140
Owner or operator
SAVION INDUSTRIES (1987), LTD. (9023606)
Roles
Manufacturer
First device listed
November 29, 1995
Registered through
2026
Brand names listed
BSC101, BSC111, BSC121, BTC400/401, DB891, EBH235, ES707E, ES707FFE and more

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
September 28, 2005K051861THE SAVION INDUSTRIES MEDI-CRUISER MODEL MS777INKSubstantially EquivalentSavion Industries, Ltd.accessdata.fda.gov

Compare with other makers

Updated September 28, 2005. 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.