Honeynaps Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Honeynaps Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SOMNUM (V.1.1.2.)
2
Total
2
Cleared
0
Denied
Honeynaps Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Jun 2026. Active since 2023. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Honeynaps Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Honeynaps Co., Ltd.
2 devices