Medical Device Manufacturer · US , South Miami , FL

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

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Aemed, Inc. has 2 FDA 510(k) cleared medical devices. Based in South Miami, US.

Historical record: 2 cleared submissions from 2008 to 2014. Primary specialty: Neurology.

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

Aemed, Inc. is one of 5627 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

2 devices

1-2 of 2