Medical Device Manufacturer · US , San Francisco , CA

Tidal Medical Technologies, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Tidal Medical Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.

Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Tidal Medical Technologies, LLC Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Medicsense USA, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Tidal Medical Technologies, LLC
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