Senorx, Inc. is one of 13189 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Senorx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EnCor Enspire™Breast Biopsy System (E4115, E4230), EnCor Breast Biopsy Probe with Rinse Tube, EnCor MRI Introducer Set, EnCor Probe Introducer
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. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Senorx, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Intertek Testing Services.
FDA 510(k) Regulatory Record - Senorx, Inc.
30 devices
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
Cleared
Jul 19, 2016
EnCor MRI Introducer Set, EnCor Probe Introducer
Gastroenterology & Urology
18d
Cleared
Jun 27, 2013
STARCHMARK BREAST TISSUE MARKER
General & Plastic Surgery
21d
Cleared
Nov 20, 2009
ENCOR BREAST BIOPSY SYSTEM
Gastroenterology & Urology
7d
Cleared
Aug 19, 2009
CONTURA CAVITY MAINTENANCE CATHETER
Radiology
15d
Cleared
Sep 12, 2008
CONTURA LUMEN MARKER
Radiology
32d
Cleared
Aug 01, 2008
STARCHMARK BIOPSY SITE MARKER, MODEL STMKEC-10GSS, STMKEC-10GTR, STMKMT-11GS
General & Plastic Surgery
107d
Cleared
May 28, 2008
PROSTATE TISSUE MARKER
General & Plastic Surgery
34d
Cleared
May 02, 2008
CONTURA MLB SOURCE APPLICATOR FOR BRACHYTHERAPY
Radiology
16d
Cleared
Apr 30, 2008
CONTURA MULTI-LUMEN BALLOON SOURCE APPLICATOR FOR BRACHYTHERAPY, MODELS...
Radiology
41d
Cleared
Mar 31, 2008
GEL MARK ULTRACOR BIOPSY SITE MARKER, MODEL: GMUC-17GGP
General & Plastic Surgery
19d