Okamoto USA, Inc. - FDA 510(k) Cleared Devices

Okamoto USA, Inc. has 14 FDA 510(k) cleared obstetrics & gynecology devices. Based in Stratford, US.

Latest FDA clearance: Feb 2025. Active since 1987.

Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hyman, Phelps & McNamara, P.C. as regulatory consultant.