Medical Device Manufacturer · CA , Markham

Artaflex, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2024
1
Total
1
Cleared
0
Denied

Artaflex, Inc. has 1 FDA 510(k) cleared medical devices. Based in Markham, CA.

Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Artaflex, Inc. Filter by specialty or product code using the sidebar.

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