Medical Device Manufacturer · US , Phoenix , AZ

Edma Group, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Edma Group, LLC has 2 FDA 510(k) cleared medical devices. Based in Phoenix, US.

Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Shanghai Truthful Information Technology Co., Ltd. as regulatory consultant.

FDA 510(k) Regulatory Record - Edma Group, LLC
2 devices
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