Hoowon Edi Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Hoowon Edi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: 8plant Implant System
1
Total
1
Cleared
0
Denied
Hoowon Edi Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gimhae, KR.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Hoowon Edi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wise Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hoowon Edi Co., Ltd.
1 devices