Aemed, Inc. is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aemed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: StimPad OTC, AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Quality First International as regulatory consultant.
FDA 510(k) Regulatory Record - Aemed, Inc.
2 devices