Home / Companies / Heuron Co., Ltd.

Heuron Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls: 0
510(k) Clearances: 5
Inspections: 0
Compliance Actions: 0

Recent 510(k) Clearances

K-Number	Device	Date
K233247	Heuron ICH	May 15, 2024
K231642	Veuron-Brain-pAb3	October 13, 2023
K203279	Veuron-Brain-mN1	July 12, 2022
K213801	Veuron-Brain-pAb2	February 4, 2022
K203142	Veuron-Brain-pAb	January 15, 2021