Filmecc Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Filmecc Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Vassallo GT 018 Hybrid, VASSALLO GT EXT, VASSALLO GT 018 Floppy
5
Total
5
Cleared
0
Denied
Filmecc Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Hagoya-Shi, JP.
Last cleared in 2023. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Filmecc Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by CardioMed Device Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Filmecc Co., Ltd.
5 devices