Medical Device Manufacturer · US , Rogers , AR

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

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Efofex, Inc. has 2 FDA 510(k) cleared medical devices. Based in Rogers, US.

Latest FDA clearance: Feb 2026. Active since 2023. Primary specialty: General Hospital.

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

Regulatory submissions have been managed by Mdi Consultants and Mdi Consultants, Inc..

FDA 510(k) Regulatory Record - Efofex, Inc.
2 devices
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