Medical Device Manufacturer · US , Louisville , KY

Induction Therapies, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Induction Therapies, LLC has 1 FDA 510(k) cleared medical devices. Based in Louisville, US.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Technology Sciences Group, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Induction Therapies, LLC
1 devices
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