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Data / Medical devices / United States / Vektor Medical, Inc.

Vektor Medical, Inc.: FDA-registered device maker in San Diego, CA, United States, 2 510(k) clearances

Vektor Medical, Inc. is registered with the FDA (registration 3021016555) in San Diego, CA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated December 4, 2025. 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
3021016555
Address
9255 Towne Centre Dr Ste 840, San Diego, CA, United States, 92121
Owner or operator
Vektor Medical Inc. (10083473)
Roles
Complaint file establishment, Manufacturer, Specification developer
First device listed
November 23, 2021
Registered through
2026
Brand names listed
Vektor Computational ECG Mapping System (vMap)

Devices it lists

DeviceProduct codeClassRoleSource
Computer, Diagnostic, ProgrammableDQK2Complaint file establishment, Manufacturer, Specification developeraccessdata.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
December 4, 2025K252429Vektor Computational ECG Mapping System (vMap®)DQKSubstantially EquivalentVektor Medical, Inc.accessdata.fda.gov
November 9, 2021K211546Vektor Computational ECG Mapping System (vMap)DQKSubstantially EquivalentVektor Medical, Inc.accessdata.fda.gov

Compare with other makers

Updated December 4, 2025. 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.