Medical Device Manufacturer · JP , Hagoya-Shi

Filmecc Co., Ltd. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2021

Recent clearances: CROSSLEAD Standard 035 and CROSSLEAD Stiff 035, Vassallo GT 018 Hybrid, VASSALLO GT EXT

6
Total
6
Cleared
0
Denied

Filmecc Co., Ltd. has 6 FDA 510(k) cleared medical devices. Based in Hagoya-Shi, JP.

Latest FDA clearance: Sep 2026. 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.

Regulatory submissions have been managed by CardioMed Device Consultants, LLC and Cardiomed Device Consultants.

FDA 510(k) Regulatory Record - Filmecc Co., Ltd.

6 devices
1-6 of 6
Filters
All6 Cardiovascular 6