Ebi, Inc. is one of 12985 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ebi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Internal Hex Implant System, Internal Octa Implant System, EBI External Implant System
4
Total
4
Cleared
0
Denied
Ebi, Inc. has 4 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 4 cleared submissions from 2008 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ebi, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Withus Group, Inc. and Withus Consulting.
FDA 510(k) Regulatory Record - Ebi, Inc.
4 devices