Aemed, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aemed, Inc. - FDA 510(k) Cleared Devices
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.
Aemed, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Dec 18, 2014
StimPad OTC
Neurology
87d
Cleared
Mar 13, 2008
AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999
Neurology
328d