Medical Device Manufacturer · US , East Lansing , MI

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

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

Avidhrt, Inc. has 1 FDA 510(k) cleared medical devices. Based in East Lansing, US.

Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Cardiovascular.

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

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

FDA 510(k) Regulatory Record - Avidhrt, Inc.
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