Remed Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Remed Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ALTMS Magnetic Stimulation Therapy System, Blossom TMS Therapy System, ALTMS Magnetic Stimulation Therapy System, Talent-Pro Electromagnetic Stimulator
3
Total
3
Cleared
0
Denied
Remed Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Daejeon, KR.
Last cleared in 2022. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Remed Co., Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by K-Biotech and Allura Medical Solutions, Inc..
FDA 510(k) Regulatory Record - Remed Co., Ltd.
3 devices