Medical Device Manufacturer · CA , Sherbrooke

Imeka Solutions, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2023

Recent clearances: ANDI 2.2, ANDI 2.0, ANDI

3
Total
3
Cleared
0
Denied

Imeka Solutions, Inc. has 3 FDA 510(k) cleared medical devices. Based in Sherbrooke, CA.

Latest FDA clearance: May 2026. Active since 2023. Primary specialty: Radiology.

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

510(k) submissions have been managed by Eversana as regulatory consultant.

FDA 510(k) Regulatory Record - Imeka Solutions, Inc.

3 devices
1-3 of 3
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All3 Radiology 3