Ami, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ami, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Picosecond Nd:YAG Laser System, Fractional CO2 Surgical Laser System
3
Total
3
Cleared
0
Denied
Ami, Inc. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Jun 2024. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ami, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Braunsolutions and Braunsolutions Regulatory Group.
FDA 510(k) Regulatory Record - Ami, Inc.
3 devices