Epica International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Epica International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: See Factor CT3™, SeeFactorCT3
2
Total
2
Cleared
0
Denied
Epica International, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Latest FDA clearance: Jun 2024. Active since 2019. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Epica International, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Frank Pokrop as regulatory consultant.
FDA 510(k) Regulatory Record - Epica International, Inc.
2 devices