Mekics Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Mekics Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: HFT750U
1
Total
1
Cleared
0
Denied
Mekics Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gyeonggi-Do, KR.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mekics Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mekics Co., Ltd.
1 devices