Medexel Co.,Ltd is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Medexel Co.,Ltd - FDA 510(k) Cleared Devices
Recent clearances: TopFine® LDS (Low Dead Space) Syringe (2 models (TS-LDS2334, TS-LDS2534)), Autokeeper
3
Total
3
Cleared
0
Denied
Medexel Co.,Ltd has 3 FDA 510(k) cleared medical devices. Based in Anseong-Si, KR.
Latest FDA clearance: Mar 2024. Active since 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medexel Co.,Ltd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Plusglobal as regulatory consultant.
FDA 510(k) Regulatory Record - Medexel Co.,Ltd
3 devices