Dreambrands, Inc. - FDA 510(k) Cleared Devices

Dreambrands, Inc. has 1 FDA 510(k) cleared medical devices. Based in Phoenix, US.

Last cleared in 2021. Active since 2021. Primary specialty: Obstetrics & Gynecology.

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

510(k) submissions have been managed by Wagoner Consulting Llg as regulatory consultant.