FMD Co., Ltd. is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.
FMD Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: FMD Peripheral Guide Wire F-14 Flex 6, FMD Peripheral Guide Wire F-18 Flex 400 (CSU415400259), FMD Peripheral Guide Wires F-14 and F-18, FMD Guide Wire Extension F-14 EXT
3
Total
3
Cleared
0
Denied
FMD Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Shibuya-Ku, JP.
Latest FDA clearance: Mar 2026. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by FMD Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - FMD Co., Ltd.
3 devices