Jeisys Medical Incorporated is one of 440 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: Potenza Prime, TRI-BEAM PRO, TRI-BEAM (Nd:YAG Laser unit), DENSITY
4
Total
4
Cleared
0
Denied
Jeisys Medical Incorporated has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Sep 2026. 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, Iqvia and Hoy & Associates Regulatory Consulting, LLC.
FDA 510(k) Regulatory Record - Jeisys Medical Incorporated
4 devices