Finemec Co., Ltd. is one of 419 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Finemec Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Nobleen Long Pulsed Alexandrite & Nd: YAG Laser System, Noblex Long Pulse Alexandrite Laser
2
Total
2
Cleared
0
Denied
Finemec Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Historical record: 2 cleared submissions from 2015 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Finemec Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lsk Biopartners, Inc. and Mcgrail Consulting, LLC.
FDA 510(k) Regulatory Record - Finemec Co., Ltd.
2 devices