Medical Device Manufacturer · US , Chester Springs , PA

Ue Lifesciences, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2012

Recent clearances: iBreastExam

Total

Cleared

Denied

Ue Lifesciences, Inc. has 3 FDA 510(k) cleared medical devices. Based in Chester Springs, US.

Historical record: 3 cleared submissions from 2012 to 2019. Primary specialty: Obstetrics & Gynecology.

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

Ue Lifesciences, 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 - Ue Lifesciences, Inc.

3 devices

1-3 of 3