Annes Daye, Ltd. - FDA 510(k) Cleared Devices

Annes Daye, Ltd. has 1 FDA 510(k) cleared medical devices. Based in London, GB.

Last cleared in 2023. Active since 2023. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by Heyer Regulatory Solutions, LLC as regulatory consultant.