Medical Device Manufacturer · KR , Daejeon

Remed Co., Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2021
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.

FDA 510(k) cleared devices by Remed Co., Ltd.

3 devices
1-3 of 3
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