Huinno Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Huinno Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MEMO Patch M (MPT-E08R-UNC01)
1
Total
1
Cleared
0
Denied
Huinno Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Huinno Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lighten Bridge, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Huinno Co., Ltd.
1 devices