Skip to the page

Data / Medical devices / Israel / Moving Life Ltd

Moving Life Ltd: FDA-registered device maker in Modiin Central, Israel, 1 510(k) clearance

Moving Life Ltd is registered with the FDA (registration 3012604975) in Modiin Central, Israel. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 19, 2023. 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
3012604975
Address
16 HaGanan Str, Modiin Central, Israel, 7169510
Owner or operator
Movinglife Ltd (10052809)
Roles
Contract manufacturer, Manufacturer
First device listed
October 8, 2016
Registered through
2026
Brand names listed
ATTO CLASSIC, ATTO SPORT, ATTO SPORT MAX, RiseAir

Devices it lists

DeviceProduct codeClassRoleSource
Vehicle, Motorized 3-WheeledINI2Contract manufacturer, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Manufactureraccessdata.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 19, 2023K222703ATTO Mobility Scooter (ATTO);ATTO Mobility Scooter (ATTO SPORT);ATTO Mobility Scooter (ATTO SPORT MAX)INISubstantially EquivalentMoving Life, Ltd.accessdata.fda.gov

Compare with other makers

Updated May 19, 2023. 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.