Skip to the page

Data / Medical devices / Israel / Curatronic, Ltd.

Curatronic, Ltd.: FDA-registered device maker in JERUSALEM Central, Israel, 2 510(k) clearances

Curatronic, Ltd. is registered with the FDA (registration 3004938911) in JERUSALEM Central, Israel. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated April 17, 2008. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3004938911
Address
101 Hebron Road, JERUSALEM Central, Israel, 9348001
Owner or operator
CURATRONIC, LTD. (9069104)
Roles
Manufacturer
First device listed
December 12, 2007
Registered through
2026
Brand names listed
Biomove 3000, Biomove 5000, Parmods

Devices it lists

DeviceProduct codeClassRoleSource
Massager, Therapeutic, ElectricISA1Manufactureraccessdata.fda.gov
Stimulator, Muscle, PoweredIPF2Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 17, 2008K080787BIOMOVE 5000 SYSTEMIPFSubstantially EquivalentCuratronic, Ltd.accessdata.fda.gov
January 27, 2005K042650BIOMOVE 3000IPFSubstantially EquivalentCuratronic, Ltd.accessdata.fda.gov

Compare with other makers

Updated April 17, 2008. 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.