Daeju Meditech Engineering Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Daeju Meditech Engineering Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: NOABLE LASER, ACTIVO, AROMA GRAND
3
Total
3
Cleared
0
Denied
Daeju Meditech Engineering Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: Mar 2025. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Daeju Meditech Engineering Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Withus Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Daeju Meditech Engineering Co., Ltd.
3 devices