Medical Device Manufacturer · US , Irvine , CA

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

30 submissions · 26 cleared · Since 2000

30

Total

26

Cleared

0

Denied

Senorx, Inc. has 26 FDA 510(k) cleared medical devices. Based in Irvine, US.

Last cleared in 2023. Active since 2000.

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

FDA 510(k) cleared devices by Senorx, Inc.

2 devices

1-2 of 2

Cleared Oct 27, 2023

EnCor Enspire™Breast Biopsy System (E4115, E4230)

General & Plastic Surgery · 29d

Cleared Mar 31, 2021

EnCor Breast Biopsy Probe with Rinse Tube

General & Plastic Surgery · 27d