Helix Opco, LLC is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Helix Opco, LLC - FDA 510(k) Cleared Devices
Recent clearances: Helix Genetic Health Risk App for late-onset Alzheimer’s disease
2
Total
1
Cleared
1
Denied
Helix Opco, LLC has 1 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Helix Opco, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Helix Opco, LLC
2 devices