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

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: General & Plastic Surgery.

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

510(k) submissions have been managed by KMC, Inc. as regulatory consultant.