Filmec Co. , Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
Filmec Co. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: VASSALLO GT Crossing14, VASSALLO GT 018 G12
2
Total
2
Cleared
0
Denied
Filmec Co. , Ltd. has 2 FDA 510(k) cleared medical devices. Based in Hagoya-Shi, JP.
Last cleared in 2023. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Filmec Co. , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Cordiomed Device Consultants and Cardiomed Device Conultants, LLC.
FDA 510(k) Regulatory Record - Filmec Co. , Ltd.
2 devices