Medical Device Manufacturer · US , Louisville , CO

Sana Health

1 submissions · 0 cleared · Since 2026
1
Total
0
Cleared
1
Denied

Sana Health — FDA 510(k) Submissions

Sana Health has submitted 1 FDA 510(k) premarket notifications since 2026, of which 0 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prescription Audiovisual Stimulator (avs) For Temporary Pain Relief (adjunctive Use) . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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All1 Neurology 1