Vitacore Industries, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Vitacore Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vitaform Procedural Mask - Blue (Vitaform Blue)
1
Total
1
Cleared
0
Denied
Vitacore Industries, Inc. has 1 FDA 510(k) cleared medical devices. Based in Port Coquitlam, CA.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vitacore Industries, Inc. Filter by specialty or product code using the sidebar.
1 submission has an FDA-authorized Predetermined Change Control Plan (PCCP), indicating AI or software-based device development.
FDA 510(k) Regulatory Record - Vitacore Industries, Inc.
1 devices