Chungwoo Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Chungwoo Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CWM-930S, FIXER DV9, Retraction, CWM-910T, APOLEX Tite
2
Total
2
Cleared
0
Denied
Chungwoo Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: May 2024. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Chungwoo Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Chungwoo Co., Ltd.
2 devices