Remedi Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Remedi Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: REMEX-GR100, Remex KA6, R-Sensor, R-Sensor
3
Total
3
Cleared
0
Denied
Remedi Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Remedi Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by 510K FDA, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Remedi Co., Ltd.
3 devices