Jeisys Medical Incorporated is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Jeisys Medical Incorporated - FDA 510(k) Cleared Devices
Recent clearances: TRI-BEAM PRO, TRI-BEAM (Nd:YAG Laser unit), DENSITY, Potenza
3
Total
3
Cleared
0
Denied
Jeisys Medical Incorporated has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Oct 2025. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Jeisys Medical Incorporated Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by E & M and Iqvia.
FDA 510(k) Regulatory Record - Jeisys Medical Incorporated
3 devices