Medical Device Manufacturer · KR , Daegu

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

6 submissions · 6 cleared · Since 2022

Total

Cleared

Denied

Incore Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Daegu, KR.

Latest FDA clearance: Apr 2024. Active since 2022. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Incore Co., Ltd. Filter by specialty or product code using the sidebar.

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

6 devices

1-6 of 6