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Data / Medical devices / Canada / Vitacore Industries

Vitacore Industries: FDA-registered device maker in Port Coquitlam British Columbia, Canada, 1 510(k) clearance

Vitacore Industries is registered with the FDA (registration 3018514354) in Port Coquitlam British Columbia, Canada. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 17, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3018514354
Address
1615 Kebet Way, Port Coquitlam British Columbia, Canada, V3C5W9
Owner or operator
Vitacore Industries Inc. (10085367)
Roles
Manufacturer
First device listed
June 9, 2022
Registered through
2026
Brand names listed
CAN99 9500, Vitaform Procedural Mask - Blue (Vitaform Blue)

Devices it lists

DeviceProduct codeClassRoleSource
Mask, SurgicalFXX2Manufactureraccessdata.fda.gov
Respirator, SurgicalMSH2Manufactureraccessdata.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
September 17, 2025K251902Vitaform Procedural Mask - Blue (Vitaform Blue); Vitaform Procedural Mask with Shield (Vitaform-FS)FXXSubstantially EquivalentVitacore Industries, Inc.accessdata.fda.gov

Compare with other makers

Updated September 17, 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.