Medical Device Manufacturer · TW , Taichung City

Medifun Corporation - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medifun Corporation General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Aug 15, 2024

Medifun Safety Lancet ( MSL1 series)

General & Plastic Surgery · 58d

Cleared Nov 22, 2023

Medifun Lancing Device, Model No. LD-E1

General & Plastic Surgery · 155d

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 11, 2026