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.

Meditrina, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5