Ami, Inc. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Braunsolutions Regulatory Group as regulatory consultant.
3 devices