Guangzhou Aimira Innovation Technology Co, Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Guangzhou Aimira Innovation Technology Co, Ltd. - FDA 510(k) Cleared ...
Recent clearances: Superflow Prime Treatment System (ASP-1M)
1
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1
Cleared
0
Denied
Guangzhou Aimira Innovation Technology Co, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Guangzhou, CN.
Latest FDA clearance: Nov 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Guangzhou Aimira Innovation Technology Co, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Guangzhou Aimira Innovation Technology Co, Ltd.
1 devices