Biogenesis Co., Ltd. is one of 18456 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biogenesis Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Biogensis Implant System-Kisses, BIOGENESIS IMPLANT SYSTEM
2
Total
2
Cleared
0
Denied
Biogenesis Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Biogenesis Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biogenesis Co., Ltd.
2 devices