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

Nemoto Kyorindo Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Tokyo, JP.

Latest FDA clearance: Aug 2024. Active since 2005. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Nemoto Kyorindo Co., Ltd. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.