Medical Device Manufacturer · US , Cupertino , CA

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

5 submissions · 5 cleared · Since 2019

Total

Cleared

Denied

Meditrina, Inc. has 5 FDA 510(k) cleared medical devices. Based in Cupertino, US.

Last cleared in 2023. Active since 2019. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - Meditrina, Inc.

5 devices

1-5 of 5