Sejong Medical Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Sejong Medical Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Laport, LAP-iX, LAP-iX Suction Irrigation
9
Total
9
Cleared
0
Denied
Sejong Medical Co., Ltd. has 9 FDA 510(k) cleared medical devices. Based in Paju-Si, KR.
Latest FDA clearance: Jun 2026. Active since 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sejong Medical Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by LK Consulting Group USA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sejong Medical Co., Ltd.
9 devices
Cleared
Jun 09, 2026
LAP-iX2N
General & Plastic Surgery
256d
Cleared
May 19, 2026
Laport
General & Plastic Surgery
243d
Cleared
Sep 29, 2021
LAP-iX
General & Plastic Surgery
568d
Cleared
Apr 03, 2020
LAP-iX Suction Irrigation
General & Plastic Surgery
24d
Cleared
May 18, 2018
Smoklean
General Hospital
231d
Cleared
Nov 28, 2017
LAP-iX Suction Irrigation
Obstetrics & Gynecology
60d
Cleared
Nov 21, 2017
LAP-iX
General & Plastic Surgery
53d
Cleared
Sep 25, 2017
LapBag
General & Plastic Surgery
105d
Cleared
Aug 29, 2017
Laport
General & Plastic Surgery
78d