Skip to the page

Data / Medical devices / Cyprus / Motion Informatics (CY) Ltd.

Motion Informatics (CY) Ltd.: FDA-registered device maker in Limassol, Cyprus, 2 510(k) clearances

Motion Informatics (CY) Ltd. is registered with the FDA (registration 3010583453) in Limassol, Cyprus. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated May 27, 2026. 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
3010583453
Address
Agias Fylaxeos & Zinonos Rossidi 2, 1st floor, Limassol, Cyprus, 3082
Owner or operator
MOTION INFORMATICS Ltd. (10045282)
Roles
Manufacturer, Repackager or relabeler
First device listed
November 3, 2013
Registered through
2026
Brand names listed
Stimel-03, StimelMD (SSMD) system

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, ElectrocardiographDRX2Repackager or relabeleraccessdata.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
May 27, 2026K260142StimelMD (SSMD) systemIPFSubstantially EquivalentMotion Informatics ltd.accessdata.fda.gov
July 11, 2013K130424STIMEL-03IPFSubstantially EquivalentStimel, Ltd.accessdata.fda.gov

Compare with other makers

Updated May 27, 2026. 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.