Skip to the page

Data / Medical devices / Canada / Vitaa Medical Solutions Inc

Vitaa Medical Solutions Inc: FDA-registered device maker in Montreal Quebec, Canada, 2 510(k) clearances

Vitaa Medical Solutions Inc is registered with the FDA (registration 3043625056) in Montreal Quebec, Canada. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated March 30, 2026. Registered through 2027. 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
3043625056
Address
2590 Rue de Rouen, Montreal, QC, Montreal Quebec, Canada, H2K 1M6
Owner or operator
ViTAA Medical Solutions Inc (10095239)
Roles
Complaint file establishment, Manufacturer
First device listed
February 10, 2026
Registered through
2027
Brand names listed
AiORTA - Plan, AiORTA Plan

Devices it lists

DeviceProduct codeClassRoleSource
Automated Radiological Image Processing SoftwareQIH2Complaint file establishment, Manufactureraccessdata.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
March 30, 2026K254207AiORTA - Plan v2.0QIHSubstantially EquivalentViTAA Medical Solutions, Inc.accessdata.fda.gov
October 30, 2025K250337AiORTA - PlanQIHSubstantially EquivalentViTAA Medical Solutions, Inc.accessdata.fda.gov

Compare with other makers

Updated March 30, 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.