Medimecca Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medimecca Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Honorst Implant System
4
Total
4
Cleared
0
Denied
Medimecca Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 4 cleared submissions from 2013 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Medimecca 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 - Medimecca Co., Ltd.
4 devices