Crescom Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Crescom Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MediAI-BA
2
Total
2
Cleared
0
Denied
Crescom Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Seongnam-Si, KR.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Crescom Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Crescom Co., Ltd.
2 devices