Premier North America, Inc. - FDA 510(k) Cleared Devices

Premier North America, Inc. has 6 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.

Latest FDA clearance: Mar 2024. Active since 2018. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Premier North America, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Shanghai CV Technology Co., Ltd. as regulatory consultant.