Medifun Corporation is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Medifun Corporation - FDA 510(k) Cleared Devices
Recent clearances: Medifun Safety Lancet ( MSL1 series), Medifun Lancing Device, Model No. LD-E1
2
Total
2
Cleared
0
Denied
Medifun Corporation has 2 FDA 510(k) cleared medical devices. Based in Taichung City, TW.
Latest FDA clearance: Aug 2024. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medifun Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Voler Biotech Consulting CO., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Medifun Corporation
2 devices